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Metformin Versus Sulfonylurea in Breast Cancer Risk of Diabetic Patients: A Systematic Review and Meta-Analysis 二甲双胍与磺脲类药物对糖尿病患者乳腺癌风险的影响:一项系统综述和荟萃分析
Pub Date : 2016-09-19 DOI: 10.17795/IJCP-5971
M. Moradi-Joo, Sahar Mohabbat-Bahar, Saeed Heidari, S. Davoodi, S. Sheyklo, M. Akbari
Context: Metformin has been used for diabetic patients. This medicine might decrease the risk of breast cancer. The main objective of this article was to determine the breast cancer risk in diabetic patients and its association with metformin and sulfonylurea. Evidence Acquisition: In order to gather evidences, main databases (MEDLINE, PubMed, Cochrane library, Science Direct, Trip, Google Scholar, Institute of Scientific Information (ISI), SCOPUS and EMBASE) as well as relevant websites have searched without time limitation up to June 2015. We have searched with appropriate keywords and strategies. After quality assessment of studies, consequences of risk and mortality for breast cancer have extracted. RevMan and comprehensive meta-analysis software has used, if needed, for meta-analysis. Results: A total of 423 studies, 352 studies have entered firstly and 11 studies have selected after final review. According to the signifi- cance of heterogeneity (I 2 = 94%) in these studies, meta-analysis have scrutinized by step by step removing the studies to investigate the reason of heterogeneity. So the relative risk of breast cancer was significant in favor of metformin (RR: 0.63, 95% CI (0.56 - 0.70), Pv < 0.001). Conclusions: In this study, we have concluded that the incidence of breast cancer in patients with type 2 diabetes who have used metformin might be less than who have used sulfonylurea. However, this finding should consider carefully and needed to be con- firmed with further studies.
背景:二甲双胍已被用于糖尿病患者。这种药可能会降低患乳腺癌的风险。本文的主要目的是确定糖尿病患者的乳腺癌风险及其与二甲双胍和磺脲的关系。证据获取:为收集证据,截至2015年6月,检索了主要数据库(MEDLINE, PubMed, Cochrane library, Science Direct, Trip,谷歌Scholar, Institute of Scientific Information (ISI), SCOPUS和EMBASE)以及相关网站,没有时间限制。我们用合适的关键词和策略进行了搜索。经过对研究的质量评估,得出了乳腺癌风险和死亡率的后果。如果需要,使用RevMan和综合元分析软件进行元分析。结果:共纳入423项研究,其中首次入组研究352项,终审筛选研究11项。根据这些研究异质性的显著性(i2 = 94%), meta分析对这些研究进行了逐级剔除,以探究异质性的原因。因此,二甲双胍的乳腺癌相对风险显著高于二甲双胍(RR: 0.63, 95% CI (0.56 - 0.70), Pv < 0.001)。结论:在这项研究中,我们得出结论,2型糖尿病患者中使用二甲双胍的乳腺癌发病率可能低于使用磺脲类药物的患者。然而,这一发现需要仔细考虑,并需要进一步的研究来证实。
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引用次数: 3
Symptomatic Occlusion of Internal Carotid Artery Caused by Pituitary Macro Adenoma Among the Patients Without Apoplectic Signs; Case Report and Review of the Literature 无中风征象的垂体大腺瘤所致症状性颈内动脉闭塞病例报告及文献回顾
Pub Date : 2016-09-19 DOI: 10.5812/IJCP.5301
Omidvar Rezaei, G. Sharifi, K. Ebrahimzadeh, Mohammad Hallajnejad
Introduction: Pituitary adenoma producing symptomatic carotid compression of the internal carotid artery without any apoplexy sign would be extremely rare and there was only one report regarding to this condition. Case Presentation: In this case report we have described a 57-year-old woman with a nonfunctional pituitary macro adenoma which has resulted to symptomatic internal carotid occlusion. Magnetic resonance imaging (MRI) revealed a large pituitary adenoma caused tight stenosis of right internal carotid. The patient has also experienced the transient ischemic attack which has confirmed to be the cause of internal carotid artery occlusion by this macro adenoma tumor. There was not any sign of apoplexy at the time of admission and the patient has not shown a history of pituitary adenoma. The patient then has undergone an endonasal transsphenoidal resection because of this nonfunctional pituitary adenoma. Conclusions: Pituitary macro adenoma producing symptomatic internal carotid occlusion might develop to several serious conditions including transient ischemic attack. Urgent surgical procedure might be the best approach to prevent further severe complications in such patients.
垂体腺瘤产生颈内动脉压迫症状而无卒中征像是极为罕见的,关于此病仅有一篇报道。病例介绍:在这个病例报告中,我们描述了一个57岁的女性无功能垂体大腺瘤,导致症状性颈内动脉闭塞。磁共振显示一大垂体腺瘤引起右侧颈内动脉狭窄。患者还经历过短暂性脑缺血发作,这被证实是该大腺瘤肿瘤阻塞颈内动脉的原因。入院时无中风迹象,患者无垂体腺瘤病史。由于无功能的垂体腺瘤,患者接受了鼻内经蝶窦切除术。结论:垂体大腺瘤引起的症状性颈内动脉闭塞可发展为包括短暂性脑缺血发作在内的几种严重疾病。紧急外科手术可能是预防此类患者进一步严重并发症的最佳方法。
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引用次数: 1
Importance of Considering Rare Disorder as Eosinophilic Granuloma in Differential Diagnosis of the Common Oral Disease 将罕见疾病视为嗜酸性肉芽肿在口腔常见病鉴别诊断中的重要性
Pub Date : 2016-09-19 DOI: 10.17795/IJCP-5684
F. Maybodi, F. Owlia, M. Karbassi, A. Azam
Introduction: Eosinophilic Granuloma (EG) is one of the subsets of langerhans cell histiocytosis Oral presentation may comprise multiple alveolar lesions accompanied by bleeding, gingival inflammation and teeth mobility ,which may encourage patients to seek a dentist. Case Presentation: In this report, a case of an 18 year old male patient with multifocal lesions of EG in both jaws is presented. Conclusions: Although LCH remains an enigma for clinicians to date because of its ambiguous presentations, but timelydiagnosis could be critical for prognosis. And dentists could have an important role in diagnosis of rare disorders like EG.
简介:嗜酸性肉芽肿(EG)是朗格汉斯细胞组织细胞增生症的一个亚群。口腔表现可能包括多个牙槽病变,并伴有出血、牙龈炎症和牙齿活动,这可能促使患者寻求牙医。病例介绍:在这个报告中,一个18岁的男性患者多局灶性病变EG在双颌提出。结论:尽管LCH的临床表现模糊不清,至今仍是一个谜,但及时诊断对预后至关重要。牙医可能在诊断EG等罕见疾病方面发挥重要作用。
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引用次数: 0
Fertility: A Control Factor for Post Mastectomy Pain Syndrome in Breast Cancer Patients 生育能力:乳腺癌患者乳房切除术后疼痛综合征的控制因素
Pub Date : 2016-09-18 DOI: 10.17795/IJCP-5119
M. Hashemian, Mohammad Reza Aflatoonian, Behnaz Aflatoonian, M. Akbari, A. Akbari
Background: Normally, surgery is the first choice of treatment for breast cancer which brings about side eects as chronic pain. Post mastectomy pain syndrome (PMPS) is one of the most prevalent side eects in breast cancer survivors as a chronic neuropathic pain lasting more than three months. The precise mechanisms and risk factors connected to chronic pain after breast surgery are not identified. Objectives: This study is aimed at identifying the eects of fertility on PMPS after breast surgery in breast cancer patients. Methods: In this case-control study, a total number of 111 women were studied. Of these, 56 women were diagnosed with positive PMPS and place in the case group, and 55 patients without pain were selected as the control group. The patients' demographic and clinical information were collected by means of a questionaire and their medical files. Descriptive statistics and inferential statistics, chi-square, Mann-whitney U, Regression Logisitic (Backward), were used to analyze the data in SPSS 22 software. Results: According to the acquired results, the mean age of the study population was 49.77 10.94, the mean weight was 69.5 11.45 kg, the mean height was 160 8.14 centimeter and mean BMI was 27.4 5.4. All in all, the results showed that fertile women were more likely not to suer from PMPS compared to nulipar women, and there was not a correlation between psychological disorders
背景:通常情况下,手术是治疗乳腺癌的首选,但其副作用是慢性疼痛。乳房切除术后疼痛综合征(PMPS)是乳腺癌幸存者中最常见的副作用之一,是一种持续超过三个月的慢性神经性疼痛。与乳房手术后慢性疼痛相关的确切机制和危险因素尚未确定。目的:本研究旨在确定生育能力对乳腺癌患者乳房手术后PMPS的影响。方法:采用病例对照研究方法,对111例妇女进行研究。其中,56名女性被诊断为PMPS阳性并被放置在病例组,55名无疼痛的患者被选择为对照组。通过问卷调查和病历资料收集患者的人口学和临床资料。在SPSS 22软件中采用描述性统计和推理统计、卡方、Mann-whitney U、回归logistic (Backward)等方法对数据进行分析。结果:根据获得的结果,研究人群的平均年龄为49.77 10.94,平均体重为69.5 11.45 kg,平均身高为160 8.14 cm,平均BMI为27.4 5.4。总而言之,结果表明,与没有生育能力的女性相比,有生育能力的女性更有可能不会因经前症候群而死亡,而且心理障碍与经前症候群之间没有关联
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引用次数: 0
Combined Application of Phosphoinositide 3-Kinase and Mammalian Target of Rapamycin Inhibitors Suppresses Cell Growth and Promotes Apoptosis in Human Lung Cancer Cell Lines 磷酸肌肽3-激酶与哺乳动物雷帕霉素靶抑制剂联合应用抑制人肺癌细胞生长并促进细胞凋亡
Pub Date : 2016-09-18 DOI: 10.17795/IJCP-3433
M. Badinloo, S. E. Mahani
PI3K/Akt/mTOR would be an important intracellular signal pathway which has found to be over-activated in neoplasia. Here, the combination eect of LY294002 (PI3K inhibitor) and rapamycine (mTOR inhibitor) has evaluated in dierent human lung cancer cell lines. MTT assay has used to assess the viability of Calu-6, SK-MES-1 and A549 cancer cells. The levels of biochemical markers of apoptosis (activated caspase-3) and cell proliferation (c-Myc and cyclin D1) have evaluated by immunoblotting. The data has shown that blockade of PI3K/Akt cascade with LY294002 (0.1-100 M) resulted in growth inhibition with IC50 ranging from 7 to 35 M. LY294002 plus rapamycin (10 nM) significantly enhanced the growth inhibition rate and elevated cleaved caspase-3 in A549 and SK-MES-1 cells. Moreover, such combination therapy had a potent decreasing eect on c-Myc and cyclin D1 protein levels. Taken together, combined inhibition of PI3K/Akt/mTOR signaling has represented a promising treatment strategy for lung cancer but the eectiveness of such combination therapy has been depending on the cancer cell types.
PI3K/Akt/mTOR可能是肿瘤中过度激活的重要细胞内信号通路。本研究评估了LY294002 (PI3K抑制剂)和雷帕霉素(mTOR抑制剂)在不同人肺癌细胞系中的联合作用。MTT法已用于评估Calu-6、SK-MES-1和A549癌细胞的生存能力。免疫印迹法检测细胞凋亡生化指标(活化caspase-3)和细胞增殖指标(c-Myc和cyclin D1)水平。数据显示,用LY294002 (0.1-100 nM)阻断PI3K/Akt级联可导致生长抑制,IC50范围为7 - 35 M, LY294002加雷帕霉素(10 nM)可显著提高A549和SK-MES-1细胞的生长抑制率和裂解caspase-3水平。此外,这种联合治疗对c-Myc和cyclin D1蛋白水平有明显的降低作用。综上所述,联合抑制PI3K/Akt/mTOR信号是一种很有前景的肺癌治疗策略,但这种联合治疗的有效性取决于癌细胞类型。
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引用次数: 0
Breast cancer screening in the 3rd world, Iran as an example 第三世界的乳腺癌筛查,以伊朗为例
Pub Date : 2016-08-31 DOI: 10.17795/IJCP-8373
M. Akbari
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引用次数: 1
Metastatic Anorectal Melanoma: A Case Report 转移性肛门直肠黑色素瘤1例报告
Pub Date : 2016-08-15 DOI: 10.17795/IJCP-4756
R. Spartacus, R. Paliwal, R. Dana, Shwetha Mutha, P. Bhatt, Anees Malavat
Introduction: Anorectal melanoma is a rare and aggressive malignancy. Patients commonly present with advanced or metastatic disease. Case Presentation: We report the case of a 60-year-old man who presented with constipation and per rectal bleeding. Abdominal CT scan showed metastasis in liver and spleen along with disease spread in inguinal, iliac and abdominal lymph nodes. He was treated with single agent Dacarbazine and ultimately succumbed to the disease. Conclusions: Anorectal melanoma remains a disease with dismal prognosis especially when the patient presents with distant metastasis.
肛肠黑色素瘤是一种罕见的恶性肿瘤。患者通常表现为晚期或转移性疾病。病例介绍:我们报告的情况下,60岁的男子谁提出便秘和直肠出血。腹部CT显示肝脏及脾脏转移,并扩散至腹股沟、髂及腹部淋巴结。他接受了单药达卡巴嗪的治疗,最终死于这种疾病。结论:肛肠黑色素瘤仍然是一种预后不佳的疾病,特别是当患者出现远处转移时。
{"title":"Metastatic Anorectal Melanoma: A Case Report","authors":"R. Spartacus, R. Paliwal, R. Dana, Shwetha Mutha, P. Bhatt, Anees Malavat","doi":"10.17795/IJCP-4756","DOIUrl":"https://doi.org/10.17795/IJCP-4756","url":null,"abstract":"Introduction: Anorectal melanoma is a rare and aggressive malignancy. Patients commonly present with advanced or metastatic disease. Case Presentation: We report the case of a 60-year-old man who presented with constipation and per rectal bleeding. Abdominal CT scan showed metastasis in liver and spleen along with disease spread in inguinal, iliac and abdominal lymph nodes. He was treated with single agent Dacarbazine and ultimately succumbed to the disease. Conclusions: Anorectal melanoma remains a disease with dismal prognosis especially when the patient presents with distant metastasis.","PeriodicalId":73510,"journal":{"name":"Iranian journal of cancer prevention","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68180839","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Malignant Tumors of Tongue in Iranian Population 伊朗人舌部恶性肿瘤
Pub Date : 2016-08-01 DOI: 10.17795/ijcp-4467
M. Akbari, S. Atarbashi Moghadam, F. Atarbashi Moghadam, Zahra Bastani
Background The incidence of oral cancers varies from one country to another, which can be clarified by the difference in the distribution of the risk factors and the possible etiologies. Tongue is a main segment of oral cavity and malignant lesions of this region accounts for nearly 30% of all oral cancers. Objectives In the present study, we evaluated the pattern of tongue cancer in Iranian population and compared these findings with those previously reported in the other countries. Methods In this multicenter, retrospective cross-sectional study recorded cases of the malignant tongue tumors in the cancer research center (CRC) of Shahid Beheshti University of Medical Sciences were extracted. The patient records and their microscopic reports were retrieved from the archives and age, sex and microscopic types were evaluated. It is to be noted that the CRC has been serving as a cancer registry center for major hospitals all over the country since the year of 2003. Thus, the obtained statistics are highly reliable. Results During the years 2003 to 2008, a total number of 952 new cases of the tongue cancer were recorded in the CRC. Most cases are diagnosed in the sixth and seventh decades of life. 450 cases (47.2%) occurred in men and 489 cases (51.36%) in women. Four different types of malignant lesions (epithelial, salivary gland, hematopoietic and mesenchymal) were diagnosed. Epithelial tumors were the most prevalent malignancies (93%) of which squamous cell carcinoma (SCC) made up 87.39% of all lesions. Salivary gland tumors had the second place with 3.15% of the total lesions. Conclusions In Iranian population, squamous cell carcinoma is the most prevalent malignancy of tongue and it is notable that the ratio of female to male population was equal. These lesions were prevalent in the sixth and seventh decades of life. Thus screening examination of tongue by dentist especially in elderly patients is necessary for early detection of cancerous lesions.
背景口腔癌的发病率因国家而异,其危险因素的分布和可能的病因也不同。舌是口腔的主要部位,其恶性病变占口腔癌的近30%。在本研究中,我们评估了伊朗人群舌癌的模式,并将这些发现与其他国家先前报道的结果进行了比较。方法对沙希德·贝赫什蒂医科大学肿瘤研究中心(CRC)的舌恶性肿瘤病例进行多中心回顾性横断面研究。从档案中检索患者记录和显微镜报告,并对年龄、性别和显微镜类型进行评估。值得注意的是,儿童权利中心自2003年以来一直是全国各大医院的癌症登记中心。因此,获得的统计数据是高度可靠的。结果2003 ~ 2008年,结直肠癌共发生舌癌新发病例952例。大多数病例在生命的第六和第七十年被诊断出来。男性450例(47.2%),女性489例(51.36%)。诊断出四种不同类型的恶性病变(上皮、唾液腺、造血和间充质)。上皮性肿瘤是最常见的恶性肿瘤(93%),其中鳞状细胞癌(SCC)占所有病变的87.39%。涎腺肿瘤次之,占病变总数的3.15%。结论在伊朗人群中,鳞状细胞癌是最常见的舌恶性肿瘤,且男女比例相当。这些病变普遍存在于六、七十岁。因此,早期发现癌性病变,尤其对老年患者,由牙医进行舌部筛检是必要的。
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引用次数: 9
Alanine to Serine Variant at Position 986 of Calcium Sensing Receptor and Colorectal Cancer Risk 钙敏感受体986位丙氨酸-丝氨酸变异与结直肠癌风险
Pub Date : 2016-08-01 DOI: 10.17795/ijcp-8098
R. Dabiri, T. Mahmoudi, H. Farahani, H. Nobakht, M. Zali
Background With regard to the effect of calcium against colorectal cancer (CRC) and considering the key role of calcium sensing receptor (CaSR) in calcium homeostasis, this study investigated whether CaSR gene rs1801725 or A986S variant was associated with susceptibility to CRC risk. Methods This study was conducted as a case-control study and 303 cases with CRC and 354 controls were enrolled. All 657 subjects were genotyped for CaSR gene A986S variant using PCR-RFLP method. Results No significant difference was observed for the A986S variant of CaSR gene in either genotype or allele frequencies between the cases and the controls and this lack of difference remained non-significant even after adjustment for age, BMI, sex, smoking status, and family history of CRC. No evidence for the effect modification of the association A986S variant and CRC by BMI, sex, or tumor site was also observed. Furthermore, the risk of obesity in relation to the A986S variant in the controls and the cases was separately analyzed and we observed no significant difference between normal weight (BMI < 25kg/m2) and overweight/obese (BMI ≥ 25kg/m2) subjects. Conclusions Our findings do not support a role for effect of the CaSR gene A986S variant on CRC risk; nevertheless, this finding requires confirmation and the role of the gene variant in carcinogenesis needs to be further investigated.
背景针对钙对结直肠癌(CRC)的作用,考虑到钙敏感受体(CaSR)在钙稳态中的关键作用,本研究探讨了CaSR基因rs1801725或A986S变异是否与结直肠癌的易感性相关。方法本研究采用病例-对照研究,纳入结直肠癌患者303例,对照组354例。采用PCR-RFLP方法对657例受试者进行CaSR基因A986S变异分型。结果CaSR基因A986S变异的基因型和等位基因频率在病例和对照组之间没有显著差异,即使在调整了年龄、BMI、性别、吸烟状况和CRC家族史后,这种差异仍然不显著。没有证据表明A986S变异与CRC的关联会因BMI、性别或肿瘤部位而改变。此外,我们还分别分析了正常体重(BMI < 25kg/m2)和超重/肥胖(BMI≥25kg/m2)受试者中A986S变异与肥胖风险的关系,结果发现正常体重(BMI < 25kg/m2)与超重/肥胖(BMI≥25kg/m2)受试者之间无显著差异。结论:我们的研究结果不支持CaSR基因A986S变异在结直肠癌风险中的作用;然而,这一发现还有待证实,该基因变异在癌变中的作用还有待进一步研究。
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引用次数: 2
Are Estrogen Receptor Genomic Aberrations Predictive of Hormone Therapy Response in Breast Cancer? 雌激素受体基因组畸变能预测乳腺癌激素治疗反应吗?
Pub Date : 2016-08-01 DOI: 10.17795/ijcp-6565
S. Tabarestani, M. Motallebi, M. Akbari
Context Breast cancer is the most common cancer in women worldwide. Estrogen receptor (ER) positive breast cancer constitutes the majority of these cancers. Hormone therapy has significantly improved clinical outcomes for early- and late-stage hormone receptor positive breast cancer. Although most patients with early stage breast cancer are treated with curative intent, approximately 20% - 30% of patients eventually experience a recurrence. During the last two decades, there have been tremendous efforts to understand the biological mechanisms of hormone therapy resistance, with the ultimate goal of implementing new therapeutic strategies to improve the current treatments for ER positive breast cancer. Several mechanisms of hormone therapy resistance have been proposed, including genetic alterations that lead to altered ER expression or ERs with changed protein sequence. Evidence Acquisition A Pubmed search was performed utilizing various related terms. Articles over the past 20 years were analyzed and selected for review. Results On the basis of published studies, the frequencies of ESR1 (the gene encoding ER) mutations in ER positive metastatic breast cancer range from 11% to 55%. Future larger prospective studies with standardized mutation detection methods may be necessary to determine the true incidence of ESR1 mutations. ESR1 amplification in breast cancer remains a controversial issue, with numerous studies either confirmed or challenged the reports of ESR1 amplification. The combination of intra-tumor heterogeneity regarding ESR1 copy number alterations and low level ESR1 copy number increase may account for these discrepancies. Conclusions While numerous unknown issues on the role of ESR1 mutations in advanced breast cancer remain, these new findings will certainly deepen current knowledge on molecular evolution of breast cancer and acquired resistance to hormone therapy.
乳腺癌是全世界女性中最常见的癌症。雌激素受体(ER)阳性乳腺癌构成了这些癌症的大多数。激素治疗显著改善了早期和晚期激素受体阳性乳腺癌的临床结果。虽然大多数早期乳腺癌患者的治疗目的是治愈,但大约20% - 30%的患者最终会复发。在过去的二十年里,人们已经付出了巨大的努力来了解激素治疗抵抗的生物学机制,最终目标是实施新的治疗策略来改善目前对雌激素受体阳性乳腺癌的治疗。已经提出了激素治疗耐药的几种机制,包括导致内质网表达改变或内质网蛋白序列改变的遗传改变。利用各种相关术语进行Pubmed检索。对过去20年的文章进行了分析和选择。结果根据已发表的研究,在ER阳性转移性乳腺癌中,ESR1(编码ER的基因)突变的频率为11% ~ 55%。未来可能需要使用标准化突变检测方法进行更大规模的前瞻性研究,以确定ESR1突变的真实发生率。乳腺癌中的ESR1扩增仍然是一个有争议的问题,许多研究证实或质疑ESR1扩增的报道。肿瘤内ESR1拷贝数改变的异质性和低水平的ESR1拷贝数增加可能解释了这些差异。尽管ESR1突变在晚期乳腺癌中的作用仍有许多未知问题,但这些新发现必将加深目前对乳腺癌分子进化和获得性激素治疗耐药的认识。
{"title":"Are Estrogen Receptor Genomic Aberrations Predictive of Hormone Therapy Response in Breast Cancer?","authors":"S. Tabarestani, M. Motallebi, M. Akbari","doi":"10.17795/ijcp-6565","DOIUrl":"https://doi.org/10.17795/ijcp-6565","url":null,"abstract":"Context Breast cancer is the most common cancer in women worldwide. Estrogen receptor (ER) positive breast cancer constitutes the majority of these cancers. Hormone therapy has significantly improved clinical outcomes for early- and late-stage hormone receptor positive breast cancer. Although most patients with early stage breast cancer are treated with curative intent, approximately 20% - 30% of patients eventually experience a recurrence. During the last two decades, there have been tremendous efforts to understand the biological mechanisms of hormone therapy resistance, with the ultimate goal of implementing new therapeutic strategies to improve the current treatments for ER positive breast cancer. Several mechanisms of hormone therapy resistance have been proposed, including genetic alterations that lead to altered ER expression or ERs with changed protein sequence. Evidence Acquisition A Pubmed search was performed utilizing various related terms. Articles over the past 20 years were analyzed and selected for review. Results On the basis of published studies, the frequencies of ESR1 (the gene encoding ER) mutations in ER positive metastatic breast cancer range from 11% to 55%. Future larger prospective studies with standardized mutation detection methods may be necessary to determine the true incidence of ESR1 mutations. ESR1 amplification in breast cancer remains a controversial issue, with numerous studies either confirmed or challenged the reports of ESR1 amplification. The combination of intra-tumor heterogeneity regarding ESR1 copy number alterations and low level ESR1 copy number increase may account for these discrepancies. Conclusions While numerous unknown issues on the role of ESR1 mutations in advanced breast cancer remain, these new findings will certainly deepen current knowledge on molecular evolution of breast cancer and acquired resistance to hormone therapy.","PeriodicalId":73510,"journal":{"name":"Iranian journal of cancer prevention","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2016-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68182348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 15
期刊
Iranian journal of cancer prevention
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