Unknown

Dataset Information

0

Activation of the PERK-ATF4 pathway promotes chemo-resistance in colon cancer cells.


ABSTRACT: Colon cancer is a major health problem worldwide. While chemotherapy remains a main approach for treating late-stage colon cancer patients, most, if not all, of them will develop drug resistance and die of uncontrollable disease progression eventually. Therefore, identification of mechanism of drug resistance and development of overcoming strategy hold great significance in management of colon cancer. In this study, we discovered that activation of the PERK branch of the unfolded protein response (UPR) pathways is required for colon cancer cells to survive treatment of 5-Fluorouracil (5-FU), one of the first-line chemotherapeutics for late-stage colon cancer patients. Genetic and pharmacological inhibition of PERK or its downstream factors greatly sensitize colon cancer cells to 5-FU. Most importantly, in vivo use of PERK inhibitor synergizes with 5-FU in suppressing the growth of colon cancer cells in mouse models. In summary, our findings established a promising way to overcome resistance to chemotherapy in colon cancer.

SUBMITTER: Shi Z 

PROVIDER: S-EPMC6397152 | biostudies-literature | 2019 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Activation of the PERK-ATF4 pathway promotes chemo-resistance in colon cancer cells.

Shi Zhong Z   Yu Xiaofu X   Yuan Meiqin M   Lv Wangxia W   Feng Tingting T   Bai Rui R   Zhong Haijun H  

Scientific reports 20190301 1


Colon cancer is a major health problem worldwide. While chemotherapy remains a main approach for treating late-stage colon cancer patients, most, if not all, of them will develop drug resistance and die of uncontrollable disease progression eventually. Therefore, identification of mechanism of drug resistance and development of overcoming strategy hold great significance in management of colon cancer. In this study, we discovered that activation of the PERK branch of the unfolded protein respons  ...[more]

Similar Datasets

| S-EPMC4990291 | biostudies-literature
| S-EPMC8505706 | biostudies-literature
| S-EPMC7218438 | biostudies-literature
| S-EPMC10223906 | biostudies-literature
| S-EPMC8199104 | biostudies-literature
| S-EPMC6942794 | biostudies-literature
2024-11-10 | GSE281408 | GEO
| S-EPMC11322142 | biostudies-literature
| S-EPMC6743121 | biostudies-literature
| S-EPMC4823713 | biostudies-literature