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Hu-Qi-Zheng-Xiao Decoction Inhibits the Metastasis of Hepatocellular Carcinoma Cells by Suppressing the HIF-1α Signaling Pathway to Inhibit EMT, LCSC, and Angiogenic Process. 藿香正气水通过抑制HIF-1α信号通路来抑制EMT、LCSC和血管生成过程,从而抑制肝细胞癌细胞的转移
IF 2.9 3区 医学 Q1 Medicine Pub Date : 2024-01-01 DOI: 10.1177/15347354231226126
Xuejing Wang, Ling Yin, Mengyin Chai, Buxin Kou, Xiaoni Liu, Xiaojun Wang

Background: Hepatocellular carcinoma (HCC) is a common clinical malignant tumor of the digestive system. Hu-Qi-Zheng-Xiao (HQZX) decoction has been clinically found to prolong the survival of patients with hepatocellular carcinoma and improve the quality of patients' survival, but its antitumor biological mechanism is still unclear.

Methods: A nude mouse hollow fiber hepatocellular carcinoma model was constructed to analyze the in vivo efficacy of HQZX decoction against 7 different hepatocellular carcinoma cells. The subcutaneous graft tumor model was again validated. In vitro, the effect of HQZX decoction on the growth and metastasis of the cell line with the highest growth inhibition was evaluated. The cell line with the best efficacy response screened was again used to construct a hollow fiber hepatocellular carcinoma model and hollow fiber conduit cells were extracted to detect the expression of HIF-1α, VEGF, EMT-related molecules, LCSCs-related molecules, and to observe the density of the subcutaneous vascular network of hollow fiber conduits. The liver metastasis model of splenic injection was constructed to observe the effect of HQZX decoction on tumor metastasis.

Results: The hollow fiber hepatocellular carcinoma model was evaluated for the efficacy of HQZX decoction, and it was found to have the highest growth inhibition of LM3-luc cells. In vitro, the CCK8 assay revealed that HQZX decoction could inhibit tumor migration and invasion and promote apoptosis. In addition, the mechanism study of extracting cells from hollow fiber tubes found that HQZX decoction could inhibit metastasis-associated HIF-1α, VEGF, EMT-related molecules, and LCSCs-related molecules expression. capillary network around subcutaneous fiber tubes was reduced in the HQZX decoction gavage group of mice. It inhibited tumor metastasis in nude mice.

Conclusions: HQZX decoction inhibited the growth of a variety of hepatocellular carcinoma cells. HQZX decoction suppressed the expression of metastasis-associated VEGF, EMT-related molecules, and LCSCs-related molecules and inhibited tumor angiogenesis and growth and metastasis, which may be related to the inhibition of the HIF-1α signaling pathway. It reveals that HQZX decoction may be a promising herbal compound for anti-HCC therapy, and also reveals the accurate feasibility of the hollow fiber hepatocellular carcinoma model for in vivo pharmacodynamic evaluation and mechanism study.

背景:肝细胞癌(HCC)是临床上常见的消化系统恶性肿瘤:肝细胞癌(HCC)是临床上常见的消化系统恶性肿瘤。临床发现,藿香正气水能延长肝细胞癌患者的生存期,改善患者的生存质量,但其抗肿瘤的生物学机制尚不清楚:方法:构建裸鼠中空纤维肝癌模型,分析HQZX煎剂对7种不同肝癌细胞的体内疗效。再次验证了皮下移植肿瘤模型。在体外,评估了 HQZX 水煎剂对生长抑制率最高的细胞系的生长和转移效果。再次用筛选出的疗效反应最好的细胞系构建中空纤维肝癌模型,提取中空纤维导管细胞,检测HIF-1α、VEGF、EMT相关分子、LCSCs相关分子的表达,并观察中空纤维导管皮下血管网的密度。构建脾脏注射肝转移模型,观察HQZX煎剂对肿瘤转移的影响:结果:在中空纤维肝癌模型中,HQZX煎剂对LM3-luc细胞的生长抑制率最高。体外CCK8检测显示,HQZX煎剂能抑制肿瘤的迁移和侵袭,并促进细胞凋亡。此外,从空心纤维管中提取细胞的机理研究发现,HQZX煎剂能抑制转移相关的HIF-1α、血管内皮生长因子、EMT相关分子和LCSCs相关分子的表达。结论:HQZX煎剂能抑制裸鼠肿瘤转移:结论:HQZX 水煎剂能抑制多种肝癌细胞的生长。结论:HQZX煎剂可抑制多种肝癌细胞的生长,抑制转移相关的VEGF、EMT相关分子和LCSCs相关分子的表达,抑制肿瘤血管生成和生长转移,可能与抑制HIF-1α信号通路有关。该研究揭示了HQZX水煎剂可能是一种很有前景的抗肝癌中药复方制剂,同时也揭示了中空纤维肝癌模型用于体内药效学评价和机制研究的准确可行性。
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引用次数: 0
Oral Decoctions Based on Qi-Yin Syndrome Differentiation After Adjuvant Chemotherapy in Resected Stage ΙΙΙA Non-Small Cell Lung Cancer: A Randomized Controlled Trial. 非小细胞肺癌ΙΙA期辅助化疗后根据气阴两虚辨证论治的口服中药:随机对照试验
IF 2.9 3区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1177/15347354241268271
Yi Jiang, Fang-Fang Liu, Yu-Qing Cai, Peng Zhang, Xiao-Feng Yang, Xiang-Yan Bi, Ruo-Yan Qin, Shi Zhang, Ju-Hua Yin, Li-Ping Shen, Jia-Xiang Liu, Ling-Shuang Liu

Objective: Powerful adjuvant strategies are required to improve the survival of patients with completely resected stage ΙΙΙA non-small cell lung cancer (NSCLC). We aimed to compare the efficacy of traditional Chinese medicine (TCM) treatment versus observation after adjuvant chemotherapy in these patients.

Methods: Eligible patients were randomized 1:1 to receive either oral decoctions based on Qi-Yin syndrome differentiation (TCM group) or observation (observation group). The intervention lasted for 12 months. The primary endpoint was 1-year disease-free survival (DFS). Secondary endpoints were DFS, quality of life, regulatory T cells (Tregs), and cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) on the surface of Tregs in peripheral blood. We used EORTC QLQ-LC43 to evaluate quality of life.

Results: Between Apr 29, 2019, and Nov 11, 2021, 75 patients were randomly assigned to oral decoctions based on Qi-Yin syndrome differentiation (n = 38) or observation (n = 37). The full analysis set included 35 patients in the TCM group and 35 in the observation group. After a median follow-up of 24.2 months, oral decoctions based on Qi-Yin syndrome differentiation improved DFS compared with observation (HR 0.378, 95% CI: 0.157-0.912; P = .03). One-year DFS was 82.1% in the TCM group and 61.9% in the observation group (P = .06). Three months after randomization, scores of total health, role function, emotional function, and social function in the TCM group were higher than those in the observation group (P < .01 for all), scores of fatigue, pain, insomnia, appetite loss, constipation, cough, and chest pain were lower than those in the observation group (P < .05 for all); there was no significant difference in the proportion of Tregs between the TCM group and the observation group (P = .58); the proportion of CTLA-4+Tregs in the TCM group was lower than that in the observation group (P = .046). There were no adverse events that occurred in both groups.

Conclusions: Oral decoctions based on Qi-Yin syndrome differentiation after adjuvant chemotherapy prolonged DFS, reduced the risk of disease recurrence and metastasis, improved quality of life, and down-regulated the proportion of CTLA-4+Tregs in completely resected stage ΙΙΙA NSCLC patients.

Trial registration: Chinese Clinical Trial Register, No. ChiCTR1800019396. Date of registration: 9 November 2018.

目的:要提高完全切除的ΙΙΙA期非小细胞肺癌(NSCLC)患者的生存率,需要强有力的辅助策略。我们的目的是比较这些患者在辅助化疗后接受中医治疗与观察的疗效:符合条件的患者按 1:1 随机分配,接受根据气阴两虚分型的口服煎剂(中医组)或观察(观察组)。干预持续 12 个月。主要终点是1年无病生存期(DFS)。次要终点为DFS、生活质量、调节性T细胞(Tregs)和外周血中Tregs表面的细胞毒性T淋巴细胞相关抗原-4(CTLA-4)。我们使用EORTC QLQ-LC43评估生活质量:2019年4月29日至2021年11月11日期间,75名患者被随机分配到基于气阴两虚综合征分型的口服煎剂(n = 38)或观察(n = 37)。完整的分析集包括中药组和观察组各35名患者。中位随访24.2个月后,与观察组相比,基于气阴两虚证分型的口服煎药改善了DFS(HR 0.378,95% CI:0.157-0.912;P = .03)。中药组的一年 DFS 为 82.1%,观察组为 61.9%(P = .06)。随机分组三个月后,中医治疗组的总体健康、角色功能、情感功能和社会功能评分均高于观察组(P P = .58);中医治疗组的 CTLA-4+Tregs 比例低于观察组(P = .046)。两组患者均未出现不良反应:结论:辅助化疗后口服 "芪阴分型汤 "可延长完全切除ΙΙA期NSCLC患者的DFS,降低疾病复发和转移的风险,改善生活质量,并下调CTLA-4+Tregs的比例:中国临床试验注册,编号:ChiCTR1800019396。注册日期:2018年11月9日。
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引用次数: 0
A single-item Expectancy Measure's Validity, Reliability, and Responsiveness to Detect Changes in Clinical Efficacy Studies of Integrative Cancer Therapies: A Methodology Study. 癌症综合疗法临床疗效研究中检测变化的单项期望测量的有效性、可靠性和响应性:方法论研究。
IF 2.9 3区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1177/15347354241273944
Anna Efverman

Background: Expectations may modify outcomes. However, studies often fail to measure expectations. This raises the need for a brief valid and reliable expectancy measure.

Objectives: To study treatment expectations in individuals entering acupuncture or rest, validity and test re-test reliability of a single-item expectancy measure graded on a category scale, a Numeric Rating Scale (NRS) and a Visual Analog Scale (VAS), and to identify psychometric differences between the scales.

Method: In this methodology study, treatment expectations were measured in 363 participants before they received acupuncture (genuine traditional penetrating or non-penetrating telescopic sham acupuncture, n = 239, 98%, responded) or a control treatment involving just rest (n = 120, 100%, responded), aimed to improve level of relaxation. A treatment expectancy measure, graded on a five-grade category scale, an eight-grade NRS and a 100 mm VAS, was tested for test re-test reliability. Level of expectation and relaxation was measured at baseline, pre- and post-therapy (n = 729 expectancy measurements).

Results: The participants scheduled for acupuncture or rest believed moderately (Inter Quartile Range, IQR, moderately-much) and much (IQR moderately-much) the treatment to be effective. The Intra-Class Correlation coefficient versus Kappa coefficient between test and re-test was .868/.868 for the category scale, .820/.820 for the NRS, and .856/.854 for the VAS. The middle step "Believe moderately the treatment to be effective" was equivalent with median 4 (IQR, 3-4) on NRS and median 52 mm (IQR 42-52) on VAS. The response rates were 708 (97%) on the category scale, 707 (97%) on the NRS, and 703 (96%) on the VAS. All three scales discriminated that pre-therapy expectations were more positive in the individuals who reported an improvement in relaxation level (P < .001-.003). The VAS presented higher responsiveness to detect expectancy changes over time (71% increased expectation), compared to the NRS (52% increased) and the category scale (12% increased), P < .001.

Conclusions: Individuals entering acupuncture, or a control intervention, presented positive treatment expectations, and the expectancy measure presented satisfactory reliability, validity, high response rates, sensitiveness, and responsiveness. Integrative cancer therapy researchers who want to control for expectancy-related bias in clinical trials should consider measuring expectation using the single-item expectancy measure.

背景:期望可能会改变结果。然而,研究往往无法测量期望值。这就需要一种简短有效且可靠的期望测量方法:研究针灸或静息治疗者的治疗期望、单项期望量表的有效性和重测可靠性,该量表采用分类量表、数字评定量表(NRS)和视觉模拟量表(VAS)进行分级,并确定量表之间的心理测量差异:在这项方法学研究中,363 名参与者在接受针灸(真正的传统透入式或非透入式伸缩假针灸,n = 239,98%,应答)或仅休息的对照治疗(n = 120,100%,应答)之前,对治疗期望进行了测量,目的是提高放松水平。通过五级类别量表、八级 NRS 和 100 毫米 VAS 对治疗期望值进行分级,并对测试再测试的可靠性进行了测试。在基线、治疗前和治疗后对期望和放松程度进行了测量(n = 729 次期望测量):结果:计划接受针灸或休息治疗的受试者对治疗效果的信任度为中度(四分位数间距,IQR,中度-高度)和高度(IQR,中度-高度)。测试与复测之间的类内相关系数与卡帕系数分别为:分类量表为 0.868/.868,NRS 为 0.820/.820,VAS 为 0.856/.854。中间步骤 "适度认为治疗有效 "与 NRS 的中位数 4(IQR,3-4)和 VAS 的中位数 52 毫米(IQR,42-52)相当。分类量表的应答率为 708 (97%),NRS 为 707 (97%),VAS 为 703 (96%)。所有三个量表均显示,报告放松程度有所改善的患者在治疗前的期望值更为积极(P < .001-.003)。与 NRS(增加 52%)和类别量表(增加 12%)相比,VAS 在检测随时间推移的期望值变化方面具有更高的反应性(71% 的期望值增加),P < .001:结论:接受针灸或对照干预的患者都表现出了积极的治疗期望,期望量表具有令人满意的可靠性、有效性、高响应率、敏感性和响应性。希望在临床试验中控制预期相关偏差的癌症综合疗法研究人员应考虑使用单项预期测量法来测量预期。
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引用次数: 0
Safety of the Herbal Medicine SH003 in Patients With Solid Cancer: A Multi-Center, Single-Arm, Open-Label, Dose-Escalation Phase I Study. 中药 SH003 在实体瘤患者中的安全性:一项多中心、单臂、开放标签、剂量递增的 I 期研究
IF 2.9 3区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1177/15347354241293451
Chunhoo Cheon, Hyun Woo Lee, Sun Jin Sym, Seong-Gyu Ko

Background: SH003, a novel herbal medicine comprising Huang-Qi, Dang-Gui, and Gua-Lou-Gen, has historical roots in traditional medicine with reported anticancer properties. The need to explore safe and effective treatments in oncology underlines the importance of this study.

Methods: This phase I trial, conducted at Ajou University Hospital and Gachon University Gil Medical Center in Korea, adopted a single-arm, open-label, dose-escalation design. It aimed to evaluate the safety of escalated doses of SH003 in patients with various solid cancers, focusing on determining its maximum tolerated dose. Participants with confirmed solid cancers, unresponsive to standard treatments, were enrolled. The dosage of SH003 was escalated from 4800 to 9600 mg per day, using a 3 + 3 design. Safety was assessed based on the Common Terminology Criteria for Adverse Events ver. 5.0.

Results: The study established that the maximum tolerated dose of SH003 is 9600 mg/day. Most adverse events were mild, primarily including dizziness and nausea, indicating the tolerability of SH003 at this dosage.

Conclusions: SH003 demonstrates safety and promises as an anticancer treatment at doses up to 9600 mg/day. This research supports further investigation into its efficacy for cancer therapy, emphasizing the significance of natural products in oncology, particularly concerning patient safety and tolerance.

背景:SH003是一种由黄芪、当归和瓜蒌根组成的新型中药,在传统医学中具有抗癌的历史渊源。探索安全有效的肿瘤治疗方法的必要性凸显了这项研究的重要性:本 I 期试验在韩国安州大学医院和嘉泉大学吉医疗中心进行,采用单臂、开放标签、剂量递增设计。试验旨在评估SH003在各种实体瘤患者中递增剂量的安全性,重点是确定其最大耐受剂量。研究人员招募了对标准治疗无效的确诊实体瘤患者。采用3+3设计,SH003的剂量从每天4800毫克递增到9600毫克。安全性根据《不良事件通用术语标准》第 5.0 版进行评估。结果:研究确定SH003的最大耐受剂量为9600毫克/天。大多数不良反应都很轻微,主要包括头晕和恶心,这表明SH003在这个剂量下是可以耐受的:结论:SH003作为一种抗癌治疗药物,在最高剂量为9600毫克/天时具有安全性和前景。这项研究支持进一步研究其在癌症治疗中的疗效,强调了天然产品在肿瘤学中的重要性,尤其是在患者的安全性和耐受性方面。
{"title":"Safety of the Herbal Medicine SH003 in Patients With Solid Cancer: A Multi-Center, Single-Arm, Open-Label, Dose-Escalation Phase I Study.","authors":"Chunhoo Cheon, Hyun Woo Lee, Sun Jin Sym, Seong-Gyu Ko","doi":"10.1177/15347354241293451","DOIUrl":"10.1177/15347354241293451","url":null,"abstract":"<p><strong>Background: </strong>SH003, a novel herbal medicine comprising Huang-Qi, Dang-Gui, and Gua-Lou-Gen, has historical roots in traditional medicine with reported anticancer properties. The need to explore safe and effective treatments in oncology underlines the importance of this study.</p><p><strong>Methods: </strong>This phase I trial, conducted at Ajou University Hospital and Gachon University Gil Medical Center in Korea, adopted a single-arm, open-label, dose-escalation design. It aimed to evaluate the safety of escalated doses of SH003 in patients with various solid cancers, focusing on determining its maximum tolerated dose. Participants with confirmed solid cancers, unresponsive to standard treatments, were enrolled. The dosage of SH003 was escalated from 4800 to 9600 mg per day, using a 3 + 3 design. Safety was assessed based on the Common Terminology Criteria for Adverse Events ver. 5.0.</p><p><strong>Results: </strong>The study established that the maximum tolerated dose of SH003 is 9600 mg/day. Most adverse events were mild, primarily including dizziness and nausea, indicating the tolerability of SH003 at this dosage.</p><p><strong>Conclusions: </strong>SH003 demonstrates safety and promises as an anticancer treatment at doses up to 9600 mg/day. This research supports further investigation into its efficacy for cancer therapy, emphasizing the significance of natural products in oncology, particularly concerning patient safety and tolerance.</p>","PeriodicalId":13734,"journal":{"name":"Integrative Cancer Therapies","volume":"23 ","pages":"15347354241293451"},"PeriodicalIF":2.9,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11528795/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142521785","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Feasibility and Usability of EnergyPoints: A Mobile Health App to Guide Acupressure Use for Cancer Symptom Management. EnergyPoints:指导使用指压疗法控制癌症症状的移动健康应用程序。
IF 2.9 3区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1177/15347354231223965
Susan L Beck, Ryan Smith, Janet Mindes, Karl Beck, JungYoon Leah Kim, Matthew Weitzman, Jennifer A M Stone, Susan Veleber, William N Dudley

Objective: To examine the feasibility and usability of EnergyPoints™, an innovative mobile health app that teaches and guides people with cancer to implement daily acupressure to self-manage their fatigue and sleep disturbances.

Methods and intervention: The study used an integrated agile, human-centered approach. Adults (age 18 years and over) with cancer experiencing at least moderate fatigue, and living in the Greater New York City community, were recruited from social media, patient advocacy groups, and referrals. Twenty participants (in 3 sprints of 3, 5, and 12) were video-recorded thinking aloud while using the app for the first time. They then used the app at home to self-administer acupressure (twice daily for 1 week) while continuously wearing a fitness tracker. Each participant completed an exit interview and modified Computer System Usability Questionnaire post-participation.

Results: Participants were ages 40 to 76 years and 65% female; 65% were non-Hispanic white. Mean pass rates per ritual exceeded 80%. Users completed (totally or partially) greater than 90% of stimulating acupressure and 70% of relaxing acupressure rituals. Sprint 3 SPs totally completed at least 1 ritual 87% of the time. The majority agreed or strongly agreed the app was easy to use (90%), easy to learn (85%), easy to understand (75%), and effective in helping perform self-acupressure (85%). In an analysis of ease of completing 5 key tasks, all successfully completed the tasks; 3 users required some assistance. Of 654 usability statements, those coded as personal experience/context (197), content related to acupressure learning (105), and content related to the onboarding/profile (71) were most frequent. The design team integrated recommendations into the app before the next sprint.

Conclusions: Findings supported feasibility and usability, as well as acceptability, and led to significant alterations and improvements. EnergyPoints™ offers an opportunity to mainstream acupressure and help cancer survivors self-manage their symptoms.

目的研究 EnergyPoints™ 的可行性和可用性,这是一款创新的移动健康应用程序,可教授并指导癌症患者每天进行穴位按摩,以自我管理疲劳和睡眠障碍:研究采用了以人为本的综合敏捷方法。研究人员通过社交媒体、患者权益组织和转介招募了至少有中度疲劳症状、居住在大纽约市社区的成人癌症患者(18 岁及以上)。对 20 名参与者(3 人、5 人和 12 人)首次使用该应用程序时的大声思考进行了视频录像。然后,他们在家使用该应用程序进行自我穴位按摩(每天两次,持续一周),同时持续佩戴健身追踪器。每位参与者都在参与后完成了退出访谈和修改后的计算机系统可用性问卷调查:参与者年龄在 40 岁至 76 岁之间,65% 为女性;65% 为非西班牙裔白人。每次仪式的平均通过率超过 80%。用户(全部或部分)完成了 90% 以上的刺激性穴位按摩和 70% 以上的放松性穴位按摩仪式。冲刺 3 SP 至少有 87% 的时间完全完成了一个仪式。大多数人同意或非常同意该应用程序易于使用(90%)、易于学习(85%)、易于理解(75%),并能有效帮助进行自我穴位按摩(85%)。在对完成 5 项关键任务的难易程度进行的分析中,所有用户都成功完成了任务;3 名用户需要一些帮助。在 654 项可用性陈述中,个人经历/背景(197 项)、与穴位按摩学习相关的内容(105 项)和与入职/档案相关的内容(71 项)最常见。设计团队在下一次冲刺之前将建议整合到了应用程序中:结论:调查结果支持可行性和可用性以及可接受性,并导致了重大的改变和改进。EnergyPoints™ 为穴位按摩主流化和帮助癌症幸存者自我管理症状提供了机会。
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引用次数: 0
The Herbal Combination Shu Gan Jie Yu Regulates the SNCG/ER-a/AKT-ERK Pathway in DMBA-Induced Breast Cancer and Breast Cancer Cell Lines Based on RNA-Seq and IPA Analysis. 基于RNA-Seq和IPA分析的中药复方舒肝解郁调控DMBA诱导的乳腺癌和乳腺癌细胞株的SNCG/ER-a/AKT-ERK通路
IF 2.9 3区 医学 Q1 Medicine Pub Date : 2024-01-01 DOI: 10.1177/15347354241233258
Yi Zhao, Linan Zhao, Tao Wang, Zhenghao Liu, Suyuan Tang, Hongxia Huang, Li Wu, Youzhi Sun

Background: Soothing the liver (called Shu Gan Jie Yu in Chinese, SGJY) is a significant therapeutic method for breast cancer in TCM. In this study, 3 liver-soothing herbs, including Cyperus rotundus L., Citrus medica L. var. sarcodactylis Swingle and Rosa rugosa Thunb. were selected and combined to form a SGJY herbal combinatory.

The aim of the study: To investigate the inhibiting effect of SGJY on breast cancer in vivo and vitro, and to explore the potential mechanisms.

Materials and methods: SGJY herbal combination was extracted using water. A breast cancer rat model was developed by chemical DMBA by gavage, then treated with SGJY for 11 weeks. The tumor tissue was preserved for RNA sequencing and analyzed by IPA software. The inhibition effects of SGJY on MCF-7 and T47D breast cancer cells were investigated by SRB assay and cell apoptosis analysis, and the protein expression levels of SNCG, ER-α, p-AKT and p-ERK were measured by western blotting.

Results: SGJY significantly reduced the tumor weight and volume, and the level of estradiol in serum. The results of IPA analysis reveal SGJY upregulated 7 canonical pathways and downregulated 16 canonical pathways. Estrogen receptor signaling was the key canonical pathway with 9 genes downregulated. The results of upstream regulator analysis reveal beta-estradiol was the central target; the upstream regulator network scheme showed that 86 genes could affect the expression of the beta-estradiol, including SNCG, CCL21 and MB. Additionally, SGJY was verified to significantly alter the expression of SNCG mRNA, CCL21 mRNA and MB mRNA which was consistent with the data of RNA-Seq. The inhibition effects of SGJY exhibited a dose-dependent response. The apoptosis rates of MCF7 and T47D cells were upregulated. The protein expression of SNCG, ER-α, p-AKT and p-ERK were all significantly decreased by SGJY on MCF-7 and T47D cells.

Conclusion: The results demonstrate that SGJY may inhibit the growth of breast cancer. The mechanism might involve downregulating the level of serum estradiol, and suppressing the protein expression in the SNCG/ER-α/AKT-ERK pathway.

背景:舒肝解郁是中医治疗乳腺癌的重要方法。本研究选择了三味舒肝理气的中药,包括香附(Cyperus rotundus L.)、枳壳(Citrus medica L. var. sarcodactylis Swingle)和蔷薇(Rosa rugosa Thunb:研究目的:研究 SGJY 在体内和体外对乳腺癌的抑制作用,并探索其潜在机制:材料和方法:用水提取 SGJY 中药复方。材料和方法:用水提取 SGJY 中药复方制剂,用化学药物 DMBA 灌胃建立乳腺癌大鼠模型,然后用 SGJY 治疗 11 周。保留肿瘤组织进行 RNA 测序,并用 IPA 软件进行分析。采用 SRB 法和细胞凋亡分析法检测 SGJY 对 MCF-7 和 T47D 乳腺癌细胞的抑制作用,并采用 Western 印迹法检测 SNCG、ER-α、p-AKT 和 p-ERK 的蛋白表达水平:结果:SGJY能明显减轻肿瘤的重量和体积,降低血清中雌二醇的水平。IPA分析结果显示,SGJY上调了7条典型通路,下调了16条典型通路。雌激素受体信号转导是关键的典型通路,有 9 个基因被下调。上游调控因子分析结果显示,β-雌二醇是中心靶标;上游调控因子网络方案显示,86 个基因可影响β-雌二醇的表达,包括 SNCG、CCL21 和 MB。此外,SGJY还能显著改变SNCG mRNA、CCL21 mRNA和MB mRNA的表达,这与RNA-Seq的数据一致。SGJY 的抑制作用表现出剂量依赖性。MCF7和T47D细胞的凋亡率上升。SGJY对MCF-7和T47D细胞中SNCG、ER-α、p-AKT和p-ERK的蛋白表达均显著降低:结果表明,SGJY 可抑制乳腺癌的生长。结论:研究结果表明,SGJY 可抑制乳腺癌的生长,其机制可能包括下调血清雌二醇水平,抑制 SNCG/ER-α/AKT-ERK 通路的蛋白表达。
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引用次数: 0
Review of Herbal Medicinal Plants Used in the Management of Cancers in the East Africa Region from 2019 to 2023. 2019年至2023年东非地区用于治疗癌症的草本药用植物回顾。
IF 2.9 3区 医学 Q1 Medicine Pub Date : 2024-01-01 DOI: 10.1177/15347354241235583
Ali Kudamba, Josephine N Kasolo, Godfrey S Bbosa, Allan Lugaajju, Henry Wabinga, Hussein M Kafeero, Jamilu E Ssenku, Shaban O Alemu, Abdul Walusansa, Nixon Niyonzima, Haruna Muwonge

Background: In the East African region, herbal plants are essential in the treatment and control of cancer. Given the diverse ecological and cultural makeup of the regional states, it is likely that different ethnic groups will use the same or different plants for the same or different diseases. However, since 2019, this has not been compiled into a single study.

Purpose: The study aimed to compile and record the medicinal plants utilized in East Africa from April 2019 to June 2023 to treat various cancer types.

Materials and methods: The study examined 13 original studies that included ethnobotanical research conducted in East Africa. They were retrieved from several internet databases, including Google Scholar, Scopus, PubMed/Medline, Science Direct, and Research for Life. The study retrieved databases on plant families and species, plant parts used, preparation methods and routes of administration, and the country where the ethnobotanical field surveys were conducted. Graphs were produced using the GraphPad Prism 8.125 program (GraphPad Software, Inc., San Diego, CA). Tables and figures were used to present the data, which had been condensed into percentages and frequencies.

Results: A total of 105 different plant species from 45 different plant families were identified, including Asteraceae (14), Euphorbiaceae (12), Musaceae (8), and Apocynaceae (7). Uganda registered the highest proportion (46% of the medicinal plants used). The most commonly mentioned medicinal plant species in cancer management was Prunus africana. Herbs (32%), trees and shrubs (28%), and leaves (45%) constituted the majority of herbal remedies. Most herbal remedies were prepared by boiling (decoction) and taken orally (57%).

Conclusion: East Africa is home to a wide variety of medicinal plant species that local populations and herbalists, or TMP, frequently use in the treatment of various types of cancer. The most frequently used families are Asteraceae and Euphorbiaceae, with the majority of species being found in Uganda. The most frequently utilized plant species is Prunus africana. Studies on the effectiveness of Prunus africana against other malignancies besides prostate cancer are required.

背景:在东非地区,草本植物对治疗和控制癌症至关重要。由于该地区各州的生态和文化构成各不相同,不同的种族群体很可能会使用相同或不同的植物来治疗相同或不同的疾病。然而,自 2019 年以来,这方面的情况尚未汇编成一份研究报告。目的:本研究旨在汇编和记录 2019 年 4 月至 2023 年 6 月期间东非地区用于治疗各种癌症的药用植物:本研究审查了 13 项原创研究,其中包括在东非开展的人种植物学研究。这些研究是从多个互联网数据库中检索的,包括谷歌学术、Scopus、PubMed/Medline、Science Direct 和 Research for Life。研究检索了有关植物科和种、所用植物部位、制备方法和给药途径以及进行民族植物学实地调查的国家的数据库。使用 GraphPad Prism 8.125 程序(GraphPad Software, Inc.)数据用表格和数字表示,并浓缩成百分比和频率:共鉴定出 45 个不同植物科的 105 种不同植物,包括菊科(14 种)、大戟科(12 种)、蕈科(8 种)和天南星科(7 种)。乌干达的比例最高(占所用药用植物的 46%)。在癌症治疗中最常提及的药用植物种类是非洲李(Prunus africana)。草药(32%)、乔木和灌木(28%)以及树叶(45%)占草药疗法的大多数。大多数草药通过煮沸(煎煮)后口服(57%):结论:东非是多种药用植物的故乡,当地居民和草药医生(TMP)经常使用这些植物治疗各种癌症。最常使用的植物科是菊科和大戟科,大部分物种在乌干达发现。最常用的植物物种是非洲李。除前列腺癌外,还需要研究非洲李对其他恶性肿瘤的疗效。
{"title":"Review of Herbal Medicinal Plants Used in the Management of Cancers in the East Africa Region from 2019 to 2023.","authors":"Ali Kudamba, Josephine N Kasolo, Godfrey S Bbosa, Allan Lugaajju, Henry Wabinga, Hussein M Kafeero, Jamilu E Ssenku, Shaban O Alemu, Abdul Walusansa, Nixon Niyonzima, Haruna Muwonge","doi":"10.1177/15347354241235583","DOIUrl":"10.1177/15347354241235583","url":null,"abstract":"<p><strong>Background: </strong>In the East African region, herbal plants are essential in the treatment and control of cancer. Given the diverse ecological and cultural makeup of the regional states, it is likely that different ethnic groups will use the same or different plants for the same or different diseases. However, since 2019, this has not been compiled into a single study.</p><p><strong>Purpose: </strong>The study aimed to compile and record the medicinal plants utilized in East Africa from April 2019 to June 2023 to treat various cancer types.</p><p><strong>Materials and methods: </strong>The study examined 13 original studies that included ethnobotanical research conducted in East Africa. They were retrieved from several internet databases, including Google Scholar, Scopus, PubMed/Medline, Science Direct, and Research for Life. The study retrieved databases on plant families and species, plant parts used, preparation methods and routes of administration, and the country where the ethnobotanical field surveys were conducted. Graphs were produced using the GraphPad Prism 8.125 program (GraphPad Software, Inc., San Diego, CA). Tables and figures were used to present the data, which had been condensed into percentages and frequencies.</p><p><strong>Results: </strong>A total of 105 different plant species from 45 different plant families were identified, including Asteraceae (14), Euphorbiaceae (12), Musaceae (8), and Apocynaceae (7). Uganda registered the highest proportion (46% of the medicinal plants used). The most commonly mentioned medicinal plant species in cancer management was <i>Prunus africana</i>. Herbs (32%), trees and shrubs (28%), and leaves (45%) constituted the majority of herbal remedies. Most herbal remedies were prepared by boiling (decoction) and taken orally (57%).</p><p><strong>Conclusion: </strong>East Africa is home to a wide variety of medicinal plant species that local populations and herbalists, or TMP, frequently use in the treatment of various types of cancer. The most frequently used families are Asteraceae and Euphorbiaceae, with the majority of species being found in Uganda. The most frequently utilized plant species is <i>Prunus africana</i>. Studies on the effectiveness of <i>Prunus africana</i> against other malignancies besides prostate cancer are required.</p>","PeriodicalId":13734,"journal":{"name":"Integrative Cancer Therapies","volume":"23 ","pages":"15347354241235583"},"PeriodicalIF":2.9,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10916491/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140039261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Prospective Multi-Centered Registry-Based Observational Study for Patients With Cancer: Design and Rationale for Korean Medicine Cancer Registry (KMCARE). 以癌症患者为对象的多中心登记为基础的前瞻性观察研究:韩国医学癌症登记处(KMCARE)的设计与原理。
IF 2.9 3区 医学 Q1 Medicine Pub Date : 2024-01-01 DOI: 10.1177/15347354231223496
Jee Young Lee, Hayun Jin, Su Bin Park, Eun Hye Kim, Jee-Hyun Yoon, Seong Woo Yoon

Background: Cancer is one of the leading causes of death in most countries with an expected increased burden on healthcare systems. Since integrative medical treatments are not collected within the scope of existing cancer registries, the establishment of the Korean Medicine Cancer Registry (KMCARE), gathering integrative therapies, including conservative care and Korean medicine, is warranted.

Methods: A prospective observational study based on the registry will be conducted in 5 Korean medical hospitals. A total of 650 eligible participants undergoing Korean medicine treatments within 1 month of a diagnosis of lung, colorectal, stomach, or breast cancer are anticipated to be enrolled in the registry. Data collected in the KMCARE can be classified into patient information, received treatments, and outcomes. The primary outcome is the Functional Assessment of Cancer Therapy-General Questionnaire score at 3 months. Secondary outcomes include the MD Anderson Symptom Inventory-Core and the Body Constitution Questionnaire at 3 and 6 months. After 6 months of follow-up periods, survival surveillance will be continued for additional 18 months. Descriptive and statistical analysis of primary and secondary outcomes, baseline data, safety, survival, and prognostic factors will be performed.

Discussion: This is the first prospective, multi-centered, registry-based observational study of cancer patients in Korean medicine hospitals, which could reveal the current status of cancer patients receiving integrative cancer therapies, and provide better insight into the role of Korean medicine in palliative care for patients with cancer.

Trial registration: Clinical Research Information Service (CRIS), KCT0007447.

背景:癌症是大多数国家的主要死因之一,预计会增加医疗系统的负担。由于现有的癌症登记处并未收集综合疗法,因此有必要建立韩国医学癌症登记处(KMCARE),收集包括保守治疗和韩国医学在内的综合疗法:方法:将在 5 家韩国医疗医院开展基于登记处的前瞻性观察研究。预计共有 650 名符合条件的参与者将在确诊肺癌、结直肠癌、胃癌或乳腺癌后 1 个月内接受韩医治疗。KMCARE 收集的数据可分为患者信息、接受的治疗和结果。主要结果是 3 个月时的癌症治疗功能评估-一般问卷得分。次要结果包括 3 个月和 6 个月时的 MD 安德森症状量表(MD Anderson Symptom Inventory-Core)和体质问卷(Body Constitution Questionnaire)。随访 6 个月后,将继续进行 18 个月的生存监测。将对主要和次要结果、基线数据、安全性、存活率和预后因素进行描述性分析和统计分析:讨论:这是首个针对韩医医院癌症患者的前瞻性、多中心、基于登记的观察性研究,可以揭示癌症患者接受癌症综合疗法的现状,更好地了解韩医在癌症患者姑息治疗中的作用:试验注册:临床研究信息服务(CRIS),KCT0007447。
{"title":"A Prospective Multi-Centered Registry-Based Observational Study for Patients With Cancer: Design and Rationale for Korean Medicine Cancer Registry (KMCARE).","authors":"Jee Young Lee, Hayun Jin, Su Bin Park, Eun Hye Kim, Jee-Hyun Yoon, Seong Woo Yoon","doi":"10.1177/15347354231223496","DOIUrl":"10.1177/15347354231223496","url":null,"abstract":"<p><strong>Background: </strong>Cancer is one of the leading causes of death in most countries with an expected increased burden on healthcare systems. Since integrative medical treatments are not collected within the scope of existing cancer registries, the establishment of the Korean Medicine Cancer Registry (KMCARE), gathering integrative therapies, including conservative care and Korean medicine, is warranted.</p><p><strong>Methods: </strong>A prospective observational study based on the registry will be conducted in 5 Korean medical hospitals. A total of 650 eligible participants undergoing Korean medicine treatments within 1 month of a diagnosis of lung, colorectal, stomach, or breast cancer are anticipated to be enrolled in the registry. Data collected in the KMCARE can be classified into patient information, received treatments, and outcomes. The primary outcome is the Functional Assessment of Cancer Therapy-General Questionnaire score at 3 months. Secondary outcomes include the MD Anderson Symptom Inventory-Core and the Body Constitution Questionnaire at 3 and 6 months. After 6 months of follow-up periods, survival surveillance will be continued for additional 18 months. Descriptive and statistical analysis of primary and secondary outcomes, baseline data, safety, survival, and prognostic factors will be performed.</p><p><strong>Discussion: </strong>This is the first prospective, multi-centered, registry-based observational study of cancer patients in Korean medicine hospitals, which could reveal the current status of cancer patients receiving integrative cancer therapies, and provide better insight into the role of Korean medicine in palliative care for patients with cancer.</p><p><strong>Trial registration: </strong>Clinical Research Information Service (CRIS), KCT0007447.</p>","PeriodicalId":13734,"journal":{"name":"Integrative Cancer Therapies","volume":"23 ","pages":"15347354231223496"},"PeriodicalIF":2.9,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10768608/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139097781","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hypothesis: Proteolytic Proenzymes Have a Role in the Ornish Program for Prostate Cancer. 假设:蛋白水解原酶在奥尼施前列腺癌治疗计划中发挥作用
IF 2.9 3区 医学 Q2 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-01-01 DOI: 10.1177/15347354241268230
Linda L Isaacs
{"title":"Hypothesis: Proteolytic Proenzymes Have a Role in the Ornish Program for Prostate Cancer.","authors":"Linda L Isaacs","doi":"10.1177/15347354241268230","DOIUrl":"10.1177/15347354241268230","url":null,"abstract":"","PeriodicalId":13734,"journal":{"name":"Integrative Cancer Therapies","volume":"23 ","pages":"15347354241268230"},"PeriodicalIF":2.9,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11292674/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141855392","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical Experience of External Application of Clearing Heat and Removing Dampness in Relieving Grade 2 to 3 Rash Caused by Programed Cell Death Protein 1 (PD-1)/Programed Cell Death Ligand 1 (PD-L1) Inhibitors: A Single-Center Retrospective Study. 清热祛湿外敷缓解程序性细胞死亡蛋白 1 (PD-1)/ 程序性细胞死亡配体 1 (PD-L1) 抑制剂引起的 2 至 3 级皮疹的临床经验:单中心回顾性研究
IF 2.9 3区 医学 Q1 Medicine Pub Date : 2024-01-01 DOI: 10.1177/15347354231226108
Shu-Yi Chen, Fang-Min Zhao, Rui Yu, Lin Sun, Yu-Dan Yin, Gao-Chen-Xi Zhang, Jia-Yao Yang, Qi-Jin Shu

Objective: In China, grade 2 to 3 immune-related rash will probably lead to the interruption of immunotherapy. Corticosteroid (CS) is the main treatment, but not always effective. The external application of clearing heat and removing dampness, which is represented by Qing-Re-Li-Shi Formula (QRLSF), has been used in our hospital to treat immune-related cutaneous adverse events (ircAEs) for the last 5 years. The purpose of this study was to discuss its efficacy and safety in the treatment of grade 2 to 3 rash.

Methods: A retrospective study of patients with grade 2 to 3 immune-related rash in our hospital from December 2019 to December 2022 was conducted. These patients received QRLSF treatment. Clinical characteristics, treatment outcome, and health-related quality of life (HrQoL) were analyzed.

Results: Thirty patients with grade 2 to 3 rash (median onset time: 64.5 days) were included. The skin lesions of 24 cases (80%) returned to grade 1 with a median time of 8 days. The accompanying symptoms were also improved with median time of 3 to 4 days. The addition of antihistamine (AH) drug didn't increase the efficacy of QRLSF (AH + QRLSF: 75.00% vs QRLSF: 83.33%, P = .66). No significant difference was observed in the efficacy of QRLSF treatment regardless of whether patients had previously received CS therapy (untreated population: 88.24% vs treated population: 69.23%, P = .36). During 1-month follow-up, 2 cases (8.33%) underwent relapses. In terms of HrQoL, QRLSF treatment could significantly reduce the median scores of all domains of Skindex-16, including symptoms (39.58 vs 8.33, P < .0001), emotions (58.33 vs 15.48, P < .0001), functioning (46.67 vs 13.33, P < .0001) and composite (52.60 vs 14.06, P < .0001).

Conclusion: External application of clearing heat and removing dampness was proven to be an effective and safe treatment for such patients. In the future, high-quality trials are required to determine its clinical application in the field of ircAEs.

目的:在中国,2 至 3 级免疫相关皮疹很可能导致免疫治疗的中断。皮质类固醇激素(CS)是主要治疗手段,但并非总是有效。以清热利湿方(QRLSF)为代表的清热利湿外敷疗法在我院用于治疗免疫相关皮肤不良反应(ircAEs)已有5年之久。本研究旨在探讨其治疗 2-3 级皮疹的有效性和安全性:方法:对我院 2019 年 12 月至 2022 年 12 月期间的 2 至 3 级免疫相关皮疹患者进行回顾性研究。这些患者接受了 QRLSF 治疗。分析了临床特征、治疗结果和健康相关生活质量(HrQoL):共纳入30例2至3级皮疹患者(中位发病时间:64.5天)。其中 24 例(80%)的皮损恢复到 1 级,中位时间为 8 天。伴随症状也有所改善,中位时间为 3 至 4 天。添加抗组胺药物(AH)并没有提高 QRLSF 的疗效(AH + QRLSF:75.00% vs QRLSF:83.33%,P = .66)。无论患者之前是否接受过 CS 治疗,QRLSF 的疗效均无明显差异(未治疗人群:88.24% vs 治疗人群:69.23%,P = .36)。在为期 1 个月的随访中,有 2 例患者(8.33%)复发。就 HrQoL 而言,QRLSF 治疗可显著降低 Skindex-16 所有领域的中位数分数,包括症状(39.58 vs 8.33,P P P P 结论:事实证明,清热祛湿外敷疗法对这类患者是一种有效而安全的治疗方法。今后需要进行高质量的试验,以确定其在 ircAEs 领域的临床应用。
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引用次数: 0
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