基因敲除
转移
结直肠癌
生物
癌症研究
自噬
癌症
体内
恶性肿瘤
细胞迁移
体外
肿瘤科
细胞凋亡
医学
生物化学
遗传学
生物技术
作者
Yu Tian,Liumei Liang,Junxiong Chen,Jiaqi Liu,Y. Su,Mengchen Shi,Weiqian Li,Shouxin Zhang,Yanchun Feng,Lingyuan He,Huanliang Liu,Xiangling Yang
标识
DOI:10.1016/j.yexcr.2023.113757
摘要
Colorectal cancer (CRC) is a common malignancy worldwide nowadays and liver metastasis is the primary cause of death in patients with CRC. Although lysosomal integral membrane protein 2 (LIMP2) has been reported to play important roles in gastric cancer and prostate cancer, its role in CRC remains unclear. The aim of this study was to investigate the function of LIMP2 in CRC invasion and migration, along with the potential underlying molecular mechanisms. We found that LIMP2 levels were higher in CRC tissues compared to adjacent normal tissues. Kaplan-Meier survival analysis showed that high expression of LIMP2 was associated with worse prognosis in CRC patients. Knockdown of LIMP2 significantly inhibited invasion, migration, and wound healing abilities of CRC cells in vitro, and inhibited CRC liver metastasis in vivo. Additionally, LIMP2 knockdown inhibited autophagy in CRC. Therefore, LIMP2 plays an important role in CRC progression. High expression of LIMP2 was associated with worse prognosis in CRC patients. Knockdown LIMP2 can effectively inhibit CRC cell migration and invasion in vitro and prevent liver metastasis in vivo. These findings suggest that LIMP2 may serve as an independent prognostic factor and potential therapeutic target for CRC.
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