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TCRP1 受 c-Myc 转录调控,赋予舌癌和肺癌的癌症化疗耐药性。

TCRP1 transcriptionally regulated by c-Myc confers cancer chemoresistance in tongue and lung cancer.

机构信息

Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Guangzhou, China.

出版信息

Sci Rep. 2017 Jun 16;7(1):3744. doi: 10.1038/s41598-017-03763-0.

DOI:10.1038/s41598-017-03763-0
PMID:28623290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5473818/
Abstract

Previously, we cloned a new gene termed 'tongue cancer resistance-associated protein 1' (TCRP1), which modulates tumorigenesis, enhances cisplatin (cDDP) resistance in cancers, and may be a potential target for reversing drug resistance. However, the mechanisms for regulating TCRP1 expression remain unclear. Herein, we combined bioinformatics analysis with luciferase reporter assay and ChIP assay to determine that c-Myc could directly bind to TCRP1 promoter to upregulate its expression. TCRP1 upregulation in multidrug resistant tongue cancer cells (Tca8113/PYM) and cisplatin-resistant A549 lung cancer cells (A549/DDP) was accompanied by c-Myc upregulation, compared to respective parental cells. In tongue and lung cancer cells, siRNA-mediated knockdown of c-Myc led to decrease TCRP1 expression, whereas overexpression c-Myc did the opposite. Moreover, TCRP1 knockdown attenuated chemoresistance resulting from c-Myc overexpression, but TCRP1 overexpression impaired the effect of c-Myc knockdown on chemosensitivity. Additionally, in both human tongue and lung cancer tissues, c-Myc protein expression positively correlated with TCRP1 protein expression and these protein levels were associated with worse prognosis for patients. Combined, these findings suggest that c-Myc could transcriptionally regulate TCRP1 in cell lines and clinical samples and identified the c-Myc-TCRP1 axis as a negative biomarker of prognosis in tongue and lung cancers.

摘要

先前,我们克隆了一个新的基因,称为“舌癌耐药相关蛋白 1”(TCRP1),它调节肿瘤发生,增强癌症的顺铂(cDDP)耐药性,可能是逆转耐药性的潜在靶标。然而,调节 TCRP1 表达的机制尚不清楚。在此,我们结合生物信息学分析与荧光素酶报告基因检测和 ChIP assay 确定 c-Myc 可以直接与 TCRP1 启动子结合以上调其表达。与相应的亲本细胞相比,多药耐药性舌癌细胞(Tca8113/PYM)和顺铂耐药性肺癌细胞(A549/DDP)中 TCRP1 的上调伴随着 c-Myc 的上调。在舌癌细胞和肺癌细胞中,siRNA 介导的 c-Myc 敲低导致 TCRP1 表达下降,而过表达 c-Myc 则相反。此外,TCRP1 敲低减弱了 c-Myc 过表达引起的化学抗性,但 TCRP1 过表达削弱了 c-Myc 敲低对化学敏感性的影响。此外,在人舌癌和肺癌组织中,c-Myc 蛋白表达与 TCRP1 蛋白表达呈正相关,这些蛋白水平与患者的预后不良相关。综上所述,这些发现表明 c-Myc 可以在细胞系和临床样本中转录调节 TCRP1,并确定了 c-Myc-TCRP1 轴作为舌癌和肺癌预后的负性生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1b/5473818/8665a6bb1e85/41598_2017_3763_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1b/5473818/5bc8d8876047/41598_2017_3763_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1b/5473818/3bacfb8f7cf4/41598_2017_3763_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1b/5473818/8665a6bb1e85/41598_2017_3763_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1b/5473818/5bc8d8876047/41598_2017_3763_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1b/5473818/3bacfb8f7cf4/41598_2017_3763_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae1b/5473818/8665a6bb1e85/41598_2017_3763_Fig3_HTML.jpg

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