MicroRNA-143-3p inhibits colorectal cancer metastases by targeting ITGA6 and ASAP3

被引:60
作者
Guo, Lingchuan [1 ]
Fu, Jianhong [2 ]
Sun, Shimei [3 ]
Zhu, Minsheng [4 ]
Zhang, Lifeng [5 ]
Niu, Hui [1 ]
Chen, Zhi [4 ]
Zhang, Yongsheng [6 ]
Guo, Lingling [1 ]
Wang, Shouli [1 ,7 ]
机构
[1] Soochow Univ, Sch Biol & Basic Med Sci, Dept Pathol, Suzhou, Peoples R China
[2] Soochow Univ, Jiangsu Inst Hematol, Affiliated Hosp 1, Suzhou, Peoples R China
[3] Peoples Hosp Sihong Cty, Dept Gastroenterol, Sihong, Peoples R China
[4] Soochow Univ, Dept Pathol, Affiliated Hosp 1, Suzhou, Peoples R China
[5] Soochow Univ, Dept Surg, Affiliated Hosp 1, Suzhou, Peoples R China
[6] Soochow Univ, Dept Pathol, Affiliated Hosp 2, Suzhou, Peoples R China
[7] Soochow Univ, Suzhou Key Lab Tumor Microenvironm & Pathol, Suzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
ASAP3; colorectal cancer; ITGA6; metastasis; miR-143-3p; BREAST-CANCER; CELL-PROLIFERATION; EXPRESSION; MIGRATION; INVASION; SUPPRESSES; INTEGRINS; PROGNOSIS; SURVIVAL; THERAPY;
D O I
10.1111/cas.13910
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs, which regulate mRNAs, operate through a variety of signaling pathways to participate in the development of colorectal cancer (CRC). In this study, we found that microRNA (miR)-143-3p expression was significantly lower in both CRC and liver metastatic CRC tissues from liver compared with normal colonic tissues. Functional assays showed that miR-143-3p inhibited CRC cell invasion and migration in vitro. Using a bioinformatics approach, we identified miR-143-3p target mRNAs. Among the candidate targets, only the expression of integrin alpha 6 (ITGA6) and ArfGAP with the SH3 domain and ankyrin repeat and PH domain 3 (ASAP3) were significantly reduced by miR-143-3p mimics as examined by western blot, and the metastasis potential of CRC cells was attenuated by endogenous ITGA6 and ASAP3 knockdown, determined by migration and invasion assays. Both ITGA6 and ASAP3 were upregulated in CRC tissues compared to normal tissues. Analysis of the relationship between clinicopathological features and ITGA6/ASAP3 protein expression in 200 patients with CRC showed a significant difference in positive ITGA6 expression between the early stage (I + II) and the advanced stage (III + IV), and ASAP3 expression levels positively correlated with metastasis in the lymph nodes. These results indicate that miR-143-3p acts as an anti-oncogene by downregulating ITGA6/ASAP3 protein expression and could offer new insight into potential therapeutic targets for CRC.
引用
收藏
页码:805 / 816
页数:12
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