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缺氧诱导因子 1α 的高表达与 NSCLC 对 EGFR 酪氨酸激酶抑制剂的获得性耐药有关。

High expression of hypoxia inducible factor 1α related with acquired resistant to EGFR tyrosine kinase inhibitors in NSCLC.

机构信息

Department of Respiratory Medicine, Tongde Hospital of Zhejiang Province, Hangzhou, Zhejiang, 310012, People's Republic of China.

Department of Respiratory Medicine, The First Hospital of Jiaxing, No. 1882 South Zhonghuan Road, Jiaxing, Zhejiang, 314000, People's Republic of China.

出版信息

Sci Rep. 2021 Jan 13;11(1):1199. doi: 10.1038/s41598-020-79801-1.

DOI:10.1038/s41598-020-79801-1
PMID:33441708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7806909/
Abstract

The acquired resistance of the first generation epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) is a main factor leading to poor prognosis of non-small cell lung cancer (NSCLC), so we researched whether the high expression of hypoxia-inducible factor-1α (HIF-1α) in EGFR-TKIs sensitive NSCLC tissue tends to induce the acquired resistance. We detected the HIF-1α in normal lung tissue, EGFR-TKIs sensitive NSCLC tissue, the first generation EGFR-TKIs acquired resistant NSCLC tissue and acquired EGFR T790M mutation NSCLC tissue with the method of immunohistochemistry. Then, we compared the expression of HIF-1α in these tissues, and evaluate the effect of HIF-1α expression to the occurrence of acquired resistance. The expression of HIF-1α was much higher in the EGFR-TKIs sensitive NSCLC tissue than that in normal lung tissue. HIF-1α level became higher after the occurrence acquired resistance. There was negative correlation between HIF-1α level before receiving treatment and the time of acquired resistance occurring as well as the acquired EGFR T790M mutation occurring. As the treatment going on, EGFR-TKIs sensitivity rate of low HIF-1α level group was much higher than that of high level group. The high expression of HIF-1α related with the acquired resistance of the first generation EGFR-TKIs, and HIF-1α can be a biomarker to predict the early occurrence of acquired resistance.

摘要

第一代表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)获得性耐药是导致非小细胞肺癌(NSCLC)预后不良的主要因素,因此我们研究了 EGFR-TKIs 敏感 NSCLC 组织中缺氧诱导因子-1α(HIF-1α)的高表达是否容易诱导获得性耐药。我们采用免疫组织化学方法检测了正常肺组织、EGFR-TKIs 敏感 NSCLC 组织、第一代 EGFR-TKIs 获得性耐药 NSCLC 组织和获得性 EGFR T790M 突变 NSCLC 组织中的 HIF-1α。然后,我们比较了这些组织中 HIF-1α 的表达,并评估了 HIF-1α 表达对获得性耐药发生的影响。EGFR-TKIs 敏感 NSCLC 组织中的 HIF-1α 表达明显高于正常肺组织。获得性耐药发生后,HIF-1α 水平升高。接受治疗前 HIF-1α 水平与获得性耐药发生时间以及获得性 EGFR T790M 突变发生时间呈负相关。随着治疗的进行,低 HIF-1α 水平组的 EGFR-TKIs 敏感性率明显高于高水平组。HIF-1α 的高表达与第一代 EGFR-TKIs 的获得性耐药有关,HIF-1α 可作为预测获得性耐药早期发生的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/b3e6782262d0/41598_2020_79801_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/601ccb50bec8/41598_2020_79801_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/ca6639445a6b/41598_2020_79801_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/71ed66e0e8cf/41598_2020_79801_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/637982f836ff/41598_2020_79801_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/b3e6782262d0/41598_2020_79801_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/601ccb50bec8/41598_2020_79801_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/ca6639445a6b/41598_2020_79801_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/71ed66e0e8cf/41598_2020_79801_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/637982f836ff/41598_2020_79801_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9869/7806909/b3e6782262d0/41598_2020_79801_Fig5_HTML.jpg

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