第一项评估结直肠癌和其他胃肠道肿瘤患者术前给予二甲双胍的安全性和对癌症干细胞影响的研究。

Cancer medicine journal Pub Date : 2021-09-01 Epub Date: 2021-02-19
Muhammad Wasif Saif, Shrikar Rajagopal, Jennifer Caplain, Martin D Goodman, Daniel Popowich, Bruce A Orkin, Philip N Tsichlis, Robert Martell
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引用次数: 0

摘要

背景:肿瘤发生的肿瘤干细胞假说认为,与肿瘤内的大多数癌细胞不同,CSC可以抵抗化疗,并在肿瘤中再生各种类型的细胞,从而导致复发。因此,选择性靶向CSC的药物可能为癌症治疗提供很大的希望,特别是当与化疗联合使用时。目前,结直肠癌(CRC)和其他胃肠道肿瘤的治疗方案依赖于手术切除、细胞毒和靶向药物的联合治疗。最近的研究结果显示,抗糖尿病药物二甲双胍与CRC风险显著降低相关(0.63 [0.47 - 0.84];P = 0.002)。因此,我们假设服用二甲双胍会减少CSC。方法:纳入结直肠癌和其他消化道肿瘤切除术患者。二甲双胍给予500毫克口服,每天两次,最多14天,并在计划手术前24小时终止。肿瘤组织和正常组织均获得。不良事件(ae)按照NCI CTCAE Version 3.0进行分级。主要目的是确定在切除前给予二甲双胍的安全性。次要目的是通过RT-PCR和免疫组织化学检测CD133、OCT4和NANOG相对mRNA水平,评估二甲双胍对CSC标志物表达的影响。结果:共10例患者(男4例;6名女性)接受二甲双胍治疗。3级ae包括贫血、低白蛋白血症、丙氨酸转氨酶升高、腹痛和恶心,但这些都与二甲双胍无关。无低血糖及乳酸性酸中毒。术后未见意外并发症。CCSC标志物比较结果显示,二甲双胍后CD133、OCT4和NANOG的表达均降低。结论:我们的初步研究显示了二甲双胍在胃肠道肿瘤手术前的可行性和对CSC的影响。这些初步数据值得在更大的随机安慰剂对照研究中进一步调查,以评估这些标志物及其与生存率的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The First Study Evaluating the Safety of Pre-Surgery Administration of Metformin in Patients with Colorectal and other Gastrointestinal Cancers and Effect on Cancer Stem Cells.

Background: The cancer stem cell (CSC) hypothesis of tumor genesis suggests that unlike most cancer cells within tumor CSC resist chemotherapy and can regenerate various cell types in tumor thereby causing relapse. Hence drugs that selectively target CSC may offer great promise for cancer therapy especially when combined with chemotherapy. Current treatment options for colorectal cancer (CRC) and other gastrointestinal (GI) tumors rely on combination of surgical resection, cytotoxic and targeted drugs. Recent findings showed that metformin, an ant diabetic drug was associated with a significantly lower risk of CRC (0.63 [0.47 - 0.84]; P = 0.002) in patients with type 2 diabetes. We therefore hypothesize that administration of metformin will reduce CSC.

Methods: Patients with CRC and other GI cancers undergoing resection were enrolled. Metformin was administered at 500 mg orally twice daily for up to 14 days and terminated 24 hours, prior to planned surgery. Both tumor and normal tissue was procured. Adverse events (AEs) were graded according to NCI CTCAE Version 3.0. Primary objective was to establish the safety of administering metformin prior to resection. Secondary objective was to evaluate the effects of metformin on the expression of CSC markers by measuring relative mRNA levels of CD133, OCT4 and NANOG by RT-PCR and immunohistochemistry.

Results: A total of 10 patients (4 Male; 6 Female) received metformin. Grade 3 AEs included anemia, hypoalbuminemia, alanine aminotransferase elevation, abdominal pain and nausea but none of these were related to metformin. No hypoglycemia and lactic acidosis were observed. No unexpected post-operative complications were witnessed. Comparison of markers of CCSC results showed that expression of CD133, OCT4 and NANOG expression were decreased following metformin.

Conclusions: Our pilot study showed feasibility of metformin before surgery in GI cancers and indicated impact on CSC. This preliminary data warrants further investigation in a larger randomized placebo-control study to assess these markers and their correlation with survival.

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