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癌相关成纤维细胞通过分泌 IL-11 靶向 JAK/STAT3/Bcl2 通路促进胃癌的化疗耐药性。

Cancer-Associated Fibroblasts Promote the Chemo-resistance in Gastric Cancer through Secreting IL-11 Targeting JAK/STAT3/Bcl2 Pathway.

机构信息

Department of Gastrointestinal and Pancreatic Surgery, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China.

Key Laboratory of Gastroenterology of Zhejiang Province, Hangzhou, China.

出版信息

Cancer Res Treat. 2019 Jan;51(1):194-210. doi: 10.4143/crt.2018.031. Epub 2018 Apr 20.

DOI:10.4143/crt.2018.031
PMID:29690750
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6333970/
Abstract

PURPOSE

Our aim was to detect the potential role of interleukin 11 (IL-11) in the development of chemo-resistance in gastric cancer and to reveal the mechanism involved in the process.

MATERIALS AND METHODS

Here, we used flow cytometry to examine the percentage of cancer-associated-fibroblasts in tumor samples from chemo-resistant and -sensitive gastric cancer patients. Using MTT assay, we detected the cell viability under different conditions. Using quantitative real-time polymerase chain reaction and Western blotting, we determined the target expressions in mRNA and protein levels. We also performed immunohistochemistry and immunofluorescence to detect the target proteins under different conditions. Animal models were constructed to verify the potential role of IL-11 in chemo-resistant develop in vivo.

RESULTS

Herein, we observed enriched cancer associated fibroblasts in drug resistant tumor tissues from gastric patients. Those fibroblasts facilitate the chemotherapeutic drugs resistance development through the secretion of IL-11, which activates the IL-11/IL-11R/gp130/ JAK/STAT3 anti-apoptosis signaling pathway in gastric cancer cells. We found that the combination of chemotherapeutic drugs and JAK inhibitor overcomes the resistance and increases the survival of mice with gastric cancer xenografts.

CONCLUSION

Our results demonstrated that IL-11 contributed to the obtain ofresistance to chemotherapy drugs through gp130/JAK/STAT3/Bcl2 pathway, and targeting the IL-11 signaling pathway induced by fibroblasts might be a promising strategy to overcome the multi-drugs resistant cancer in clinic.

摘要

目的

本研究旨在探讨白细胞介素 11(IL-11)在胃癌化疗耐药中的作用及其可能的作用机制。

材料和方法

采用流式细胞术检测化疗耐药和化疗敏感胃癌患者肿瘤组织中癌相关成纤维细胞的比例。采用 MTT 法检测不同条件下细胞的活力。采用实时定量聚合酶链反应和 Western blot 检测靶基因在 mRNA 和蛋白水平上的表达。采用免疫组化和免疫荧光法检测不同条件下的靶蛋白。构建动物模型,体内验证 IL-11 在化疗耐药发展中的潜在作用。

结果

本研究观察到胃癌耐药肿瘤组织中富含癌相关成纤维细胞。这些成纤维细胞通过分泌白细胞介素 11(IL-11)促进化疗药物耐药的发展,IL-11 通过激活胃癌细胞中的 IL-11/IL-11R/gp130/JAK/STAT3 抗凋亡信号通路发挥作用。我们发现,化疗药物与 JAK 抑制剂联合应用可克服耐药性并提高胃癌异种移植小鼠的生存率。

结论

我们的研究结果表明,IL-11 通过 gp130/JAK/STAT3/Bcl2 通路促进对化疗药物的耐药性,靶向成纤维细胞诱导的 IL-11 信号通路可能是克服临床多药耐药性癌症的一种有前途的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/d9992805735b/crt-2018-031f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/a57bfd6390c7/crt-2018-031f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/45bb83669e16/crt-2018-031f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/68c4f72abf1c/crt-2018-031f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/56c6bef7248c/crt-2018-031f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/d9992805735b/crt-2018-031f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/a57bfd6390c7/crt-2018-031f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/45bb83669e16/crt-2018-031f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/68c4f72abf1c/crt-2018-031f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/56c6bef7248c/crt-2018-031f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b033/6333970/d9992805735b/crt-2018-031f5.jpg

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The anti-apoptotic BAG3 protein is involved in BRAF inhibitor resistance in melanoma cells.抗凋亡蛋白BAG3参与黑色素瘤细胞对BRAF抑制剂的耐药性。
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Collateral Damage Intended-Cancer-Associated Fibroblasts and Vasculature Are Potential Targets in Cancer Therapy.
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