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[Corrigendum] Chloroquine potentiates the anticancer effect of sunitinib on renal cell carcinoma by inhibiting autophagy and inducing apoptosis [更正]氯喹通过抑制自噬和诱导凋亡增强舒尼替尼对肾细胞癌的抗癌作用
Pub Date : 2024-04-17 DOI: 10.3892/ol.2024.14403
Manli Li, You-zhi Xu, Wen-Jie Lu, Yong-huai Li, Shi-Sheng Tan, Hong-Jun Lin, Tian-Ming Wu, Yan Li, Si Y Wang, Ying-Lan Zhao
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引用次数: 0
A novel immune‑related lncRNA as a prognostic biomarker in HER2+ breast cancer 作为 HER2+ 乳腺癌预后生物标志物的新型免疫相关 lncRNA
Pub Date : 2024-04-16 DOI: 10.3892/ol.2024.14402
Xinwei Li, Yue Meng, Bing Gu
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引用次数: 0
Perfusion drugs for non‑muscle invasive bladder cancer (Review) 治疗非肌浸润性膀胱癌的灌注药物(综述)
Pub Date : 2024-04-15 DOI: 10.3892/ol.2024.14400
Jingyuan Qian, Qiuchen Zhang, Yang Cao, Xi Chu, Yiyang Gao, Haifei Xu, Hongzhou Cai, Jiajia Wu
The high recurrence rate and poor prognosis of non-muscle invasive bladder cancer (BC) are challenges that need to be urgently addressed. Transurethral cystectomy for bladder tumors is often combined with bladder perfusion therapy, which can effectively reduce the recurrence and progression rates of BC. The present review integrated and analyzed currently available bladder perfusion drugs, mainly including chemotherapeutic agents, immunotherapeutic agents and other adjuvant perfusion drugs. Bacillus Calmette-Guerin (BCG) perfusion was the pioneering immunotherapy for early BC and still ranks high in the selection of perfusion drugs. However, BCG infusion has a high toxicity profile and has been shown to be ineffective in some patients. Due to the limitations of BCG, new bladder perfusion drugs are constantly being developed. Immunotherapeutic agents have opened a whole new chapter in the selection of therapeutic agents for bladder perfusion. The present review explored the mechanism of action, clinical dosage and adverse effects of a variety of bladder perfusion drugs currently in common use, described combined perfusion and compared the effects of certain drugs on BC.
非肌层浸润性膀胱癌(BC)复发率高、预后差,是亟待解决的难题。膀胱肿瘤经尿道膀胱切除术常与膀胱灌注治疗相结合,可有效降低膀胱癌的复发率和进展率。本综述整合分析了目前可用的膀胱灌注药物,主要包括化疗药物、免疫治疗药物和其他辅助灌注药物。卡介苗(Bacillus Calmette-Guerin,BCG)灌注是早期 BC 免疫疗法的先驱,至今仍是灌注药物选择的首选。然而,卡介苗灌注具有较高的毒性,对一些患者已被证明无效。由于卡介苗的局限性,新的膀胱灌注药物正在不断开发中。免疫治疗药物为膀胱灌注治疗药物的选择揭开了全新的篇章。本综述探讨了目前常用的各种膀胱灌注药物的作用机制、临床用量和不良反应,介绍了联合灌注,并比较了某些药物对 BC 的影响。
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引用次数: 0
[Retracted] Upregulation of microRNA‑181b inhibits CCL18‑induced breast cancer cell metastasis and invasion via the NF‑κB signaling pathway [撤稿】通过 NF-κB 信号通路上调 microRNA-181b 可抑制 CCL18 诱导的乳腺癌细胞转移和侵袭
Pub Date : 2024-04-15 DOI: 10.3892/ol.2024.14401
Lei Wang, Yu-xia Wang, Li-Ping Chen, Ming-Li Ji
[This retracts the article DOI: 10.3892/ol.2016.5230.].
[本文撤稿,DOI: 10.3892/ol.2016.5230.]。
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引用次数: 0
Lenvatinib‑based treatment regimens in conversion therapy of unresectable hepatocellular carcinoma: A systematic review and meta‑analysis 基于伦伐替尼的治疗方案在不可切除肝细胞癌转化治疗中的应用:系统综述和荟萃分析
Pub Date : 2024-04-12 DOI: 10.3892/ol.2024.14398
Sai-sai Li, Zeyu Zhang, Zheng Wang, Kenan Wang, Minghao Sui, Dongbin Liu, Kuo Liang
Hepatocellular carcinoma (HCC) is a malignancy associated with high morbidity and mortality rates. Conversion therapy provides patients with unresectable HCC (uHCC) the opportunity to undergo radical treatment and achieve long-term survival. Despite accumulating evidence regarding the efficacy of conversion therapy, the optimal treatment approach for such therapy remains uncertain. Lenvatinib (LEN) has shown efficacy and tolerable rates of adverse events (AEs) when applied in combination with immune checkpoint inhibitors (ICIs) or locoregional therapy (LRT) over the past decade. Therefore, the present meta-analysis was performed to systematically assess the safety and efficacy of LEN-based treatment regimens in conversion therapies for uHCC. Data on outcomes, including the conversion rate, objective response rate (ORR), disease control rate (DCR) and AE incidence in patients with uHCC, were collected. A systematic literature search was performed using MEDLINE, Embase, Web of Science and Cochrane Library databases, up to the date of September 1, 2023. In total, 16 studies, encompassing a total of 1,650 cases of uHCC, were included in the final meta-analysis. The pooled conversion rates for LEN alone, LEN + ICI, LEN + LRT and LEN + ICI + LRT were calculated to be 0.04 (95% CI, 0.00–0.07; I2=77%), 0.23 (95% CI, 0.16–0.30; I2=66%), 0.14 (95% CI, 0.10–0.18; I2=0%) and 0.35 (95% CI, 0.23–0.47; I2=88%), respectively. The pooled ORRs for LEN alone, LEN + ICI, LEN + LRT and LEN + ICI + LRT were found to be 0.45 (95% CI, 0.23–0.67; I2=96%), 0.49 (95% CI, 0.39–0.60; I2=78%), 0.43 (95% CI, 0.24–0.62; I2=88%) and 0.69 (95% CI, 0.56–0.82; I2=92%), respectively. The pooled DCRs for LEN alone, LEN + ICI, LEN + LRT and LEN + ICI + LRT were observed to be 0.77 (95% CI, 0.73–0.81; I2=23%), 0.82 (95% CI, 0.69–0.95; I2=90%), 0.67 (95% CI, 0.39–0.94; I2=94%) and 0.87 (95% CI, 0.82–0.93; I2=67%), respectively. The pooled grade ≥3 AEs for LEN alone, LEN + ICI, LEN + LRT and LEN + ICI + LRT were 0.25 (95% CI, 0.14–0.36; I2=89%), 0.43 (95% CI, 0.34–0.53; I2=23%), 0.42 (95% CI, 0.19–0.66; I2=81%) and 0.35 (95% CI, 0.17–0.54; I2=94%), respectively. These findings suggested that LEN-based combination strategies may confer efficacy and acceptable tolerability for patients with uHCC. In particular, LEN + ICI, with or without LRT, appears to represent a highly effective conversion regimen, with an acceptable conversion rate and well-characterized safety profile.
肝细胞癌(HCC)是一种发病率和死亡率都很高的恶性肿瘤。转换疗法为无法切除的肝细胞癌(uHCC)患者提供了接受根治性治疗并获得长期生存的机会。尽管有关转换疗法疗效的证据不断积累,但这种疗法的最佳治疗方法仍不确定。在过去的十年中,当伦伐替尼(LEN)与免疫检查点抑制剂(ICIs)或局部区域治疗(LRT)联合应用时,已显示出疗效和可耐受的不良反应(AEs)发生率。因此,本荟萃分析旨在系统评估基于LEN的治疗方案在uHCC转换疗法中的安全性和有效性。研究收集了uHCC患者的转归率、客观反应率(ORR)、疾病控制率(DCR)和AE发生率等结果数据。我们使用 MEDLINE、Embase、Web of Science 和 Cochrane Library 数据库进行了系统性文献检索,检索时间截至 2023 年 9 月 1 日。最终的荟萃分析共纳入了16项研究,涉及1650例uHCC病例。经计算,单用LEN、LEN + ICI、LEN + LRT和LEN + ICI + LRT的集合转换率分别为0.04(95% CI,0.00-0.07;I2=77%)、0.23(95% CI,0.16-0.30;I2=66%)、0.14(95% CI,0.10-0.18;I2=0%)和0.35(95% CI,0.23-0.47;I2=88%)。单独使用 LEN、LEN + ICI、LEN + LRT 和 LEN + ICI + LRT 的汇总 ORR 分别为 0.45(95% CI,0.23-0.67;I2=96%)、0.49(95% CI,0.39-0.60;I2=78%)、0.43(95% CI,0.24-0.62;I2=88%)和 0.69(95% CI,0.56-0.82;I2=92%)。观察发现,单用LEN、LEN + ICI、LEN + LRT和LEN + ICI + LRT的集合DCR分别为0.77(95% CI,0.73-0.81;I2=23%)、0.82(95% CI,0.69-0.95;I2=90%)、0.67(95% CI,0.39-0.94;I2=94%)和0.87(95% CI,0.82-0.93;I2=67%)。单用LEN、LEN + ICI、LEN + LRT和LEN + ICI + LRT的合并≥3级AEs分别为0.25(95% CI,0.14-0.36;I2=89%)、0.43(95% CI,0.34-0.53;I2=23%)、0.42(95% CI,0.19-0.66;I2=81%)和0.35(95% CI,0.17-0.54;I2=94%)。这些研究结果表明,以LEN为基础的联合策略可为uHCC患者带来疗效和可接受的耐受性。特别是,LEN + ICI(无论是否使用LRT)似乎是一种高效的转换方案,其转换率可接受,安全性特征良好。
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引用次数: 0
Precision CT‑guided marking with India ink and microcoils for laparoscopic resection of a lateral lymph node recurrence of rectal cancer: A case report 用印度墨水和微线圈在 CT 引导下精确标记直肠癌侧淋巴结复发的腹腔镜切除术:病例报告
Pub Date : 2024-04-12 DOI: 10.3892/ol.2024.14399
Shunsuke Furukawa, Masatsugu Hiraki, Takeshi Oda, Yukihiko Takahashi, Ryuichirou Samejima
Although rarely used in laparoscopic surgery, computed tomography (CT)-guided marking is useful for targeting small lesions. The present study describes the performance of laparoscopic resection with preoperative CT-guided marking for lateral lymph node recurrence of rectal cancer. A 48-year-old man underwent laparoscopic low anterior resection with D3 lymph node dissection for rectal cancer (postoperative diagnosis, stage IIIb). Postoperative adjuvant chemotherapy was then administered. Solitary lymph node recurrence was observed in the left lateral region after 6 months. Systemic chemotherapy reduced the size of the metastatic lymph nodes; however, 3.5 years after the surgery, the diameter increased by 10 mm, and laparoscopic resection was thus planned. Because the target lesion was small and located deep in the pelvis, preoperative CT-guided marking was performed with India ink injection and embolization microcoil implantation. The markers were clearly identified and the lesion was successfully resected with adequate margins. The approach described in the present study is thus considered potentially useful for the detection of small lesions.
虽然在腹腔镜手术中很少使用,但计算机断层扫描(CT)引导下的标记对于定位小病灶非常有用。本研究描述了腹腔镜切除术术前CT引导标记治疗直肠癌侧淋巴结复发的效果。一名 48 岁的男性因直肠癌(术后诊断为 IIIb 期)接受了腹腔镜低位前切除术和 D3 淋巴结清扫术。术后进行了辅助化疗。6 个月后,在左外侧区域观察到淋巴结复发。全身化疗缩小了转移淋巴结的大小,但术后 3.5 年,淋巴结直径又增大了 10 毫米,因此计划进行腹腔镜切除术。由于靶病灶较小,且位于盆腔深处,因此术前在CT引导下进行了印度墨水注射标记和栓塞微线圈植入术。标记被清晰地识别出来,病灶被成功切除,并留有足够的边缘。因此,本研究中描述的方法被认为可用于检测小病灶。
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引用次数: 0
Bioinformatics analysis and experimental verification of NLRX1 as a prognostic factor for esophageal squamous cell carcinoma NLRX1 作为食管鳞状细胞癌预后因子的生物信息学分析和实验验证
Pub Date : 2024-04-11 DOI: 10.3892/ol.2024.14397
Lu Zhou, Lanlan Gan, Chen Sun, Alan Chu, Menglin Yang, Zongwen Liu
Nucleotide binding and oligomeric domain-like receptor X1 (NLRX1), a member of the NLR family, is associated with the physiological and pathological processes of inflammation, autophagy, immunity, metabolism and mitochondrial regulation, and has been demonstrated to have pro- or antitumor effects in various tumor types. However, the biological function of NLRX1 in esophageal squamous cell carcinoma (ESCC) has remained elusive. In the present study, by using bioinformatics methods, the differential expression of NLRX1 at the mRNA level was examined. Overall survival, clinical correlation, receiver operating characteristic curve, Cox regression, co-expression, enrichment, immune infiltration and drug sensitivity analyses were carried out. A nomogram and a calibration curve were constructed. Changes in protein expression levels were investigated by immunohistochemistry and western blotting. The impact of NLRX1 on i) cell proliferation was evaluated by Cell Counting Kit-8 assays; ii) migration was examined by wound-healing assays; iii) migration and invasion were evaluated by Transwell assays; and iv) apoptosis was assessed by Annexin V/PI staining and flow cytometry. The results revealed that, compared to normal adjacent tissue, NLRX1 was lowly expressed in ESCC, and patients with low NLRX1 expression had a shorter survival time. NLRX1 was an independent prognostic factor for ESCC and was associated with tumor grading. Patients in the low-NLRX1 group showed a decrease in the infiltration of activated natural killer cells, monocytes and M0 macrophages, and these immune-cell infiltration levels were positively correlated with NLRX1 expression. Knocking down NLRX1 promoted the proliferation of KYSE450 cells, while overexpression of NLRX1 inhibited the proliferation of ECA109 cells. NLRX1 negatively regulated the PI3K/AKT signaling pathway in ESCC. These findings indicate that, through several mechanisms, NLRX1 suppresses tumor growth in ESCC, which offers new insight for investigating the causes and progression of ESCC, as well as for identifying more efficient therapeutic approaches.
核苷酸结合和寡聚体结构域样受体X1(NLRX1)是NLR家族的成员之一,与炎症、自噬、免疫、新陈代谢和线粒体调节等生理和病理过程有关,并已被证实在多种肿瘤类型中具有促癌或抗癌作用。然而,NLRX1在食管鳞状细胞癌(ESCC)中的生物学功能一直未被发现。本研究利用生物信息学方法研究了 NLRX1 在 mRNA 水平上的差异表达。研究还进行了总生存率、临床相关性、接收器操作特征曲线、Cox 回归、共表达、富集、免疫浸润和药物敏感性分析。绘制了提名图和校准曲线。通过免疫组织化学和 Western 印迹法研究了蛋白质表达水平的变化。NLRX1对以下方面的影响:①细胞增殖(通过细胞计数试剂盒-8检测);②迁移(通过伤口愈合检测);③迁移和侵袭(通过Transwell检测);以及④凋亡(通过Annexin V/PI染色和流式细胞术检测)。结果显示,与正常邻近组织相比,NLRX1在ESCC中的表达量较低,NLRX1表达量低的患者生存时间较短。NLRX1是ESCC的独立预后因素,与肿瘤分级有关。低NLRX1组患者的活化自然杀伤细胞、单核细胞和M0巨噬细胞浸润减少,这些免疫细胞浸润水平与NLRX1表达呈正相关。敲除 NLRX1 可促进 KYSE450 细胞的增殖,而过表达 NLRX1 则会抑制 ECA109 细胞的增殖。NLRX1能负向调节ESCC中的PI3K/AKT信号通路。这些研究结果表明,NLRX1 通过多种机制抑制 ESCC 中肿瘤的生长,这为研究 ESCC 的病因和进展以及确定更有效的治疗方法提供了新的视角。
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引用次数: 0
Assessment and prognostic significance of a serum cytokine panel in diffuse large B‑cell lymphoma 弥漫大 B 细胞淋巴瘤血清细胞因子组合的评估和预后意义
Pub Date : 2024-03-28 DOI: 10.3892/ol.2024.14370
Shufang Xie, Lifen Zhu, Lei Wang, Shibing Wang, Xiangmin Tong, Wanmao Ni
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引用次数: 0
Glycolysis‑related lncRNA may be associated with prognosis and immune activity in grade II‑III glioma 糖酵解相关lncRNA可能与II-III级胶质瘤的预后和免疫活性有关
Pub Date : 2024-03-28 DOI: 10.3892/ol.2024.14371
Tao Yang, Ruiguang Zhang, Zhenfen Cui, Bowen Zheng, Xiaowei Zhu, Xinyu Yang, Qiang Huang
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引用次数: 0
Postoperative long‑term outcomes of acute normovolemic hemodilution in pancreatic cancer: A propensity score matching analysis 胰腺癌术后急性常容量血液稀释的长期疗效:倾向评分匹配分析
Pub Date : 2024-03-27 DOI: 10.3892/ol.2024.14369
T. Wakiya, K. Ishido, N. Kimura, H. Nagase, T. Kanda, Shunsuke Kubota, H. Fujita, Yoshiya Takahashi, Takeshi Yamamoto, Kohei Chida, Junichi Saito, Kazuyoshi Hirota, Kenichi Hakamada
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引用次数: 0
期刊
Oncology Letters
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