LIN28B Promotes Colon Cancer Progression and Metastasis

被引:193
作者
King, Catrina E. [1 ,2 ,5 ]
Cuatrecasas, Miriam [6 ]
Castells, Antoni [7 ]
Sepulveda, Antonia R. [3 ]
Lee, Ju-Seog [8 ,9 ]
Rustgi, Anil K. [1 ,2 ,4 ,5 ]
机构
[1] Univ Penn, Div Gastroenterol, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Pathol, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Genet, Philadelphia, PA 19104 USA
[5] Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[6] Univ Barcelona, CDB, Hosp Clin, Dept Pathol, E-08007 Barcelona, Spain
[7] Hosp Clin Barcelona, Dept Gastroenterol, CIBERehd, IDIBAPS, Barcelona, Catalonia, Spain
[8] Univ Texas MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77030 USA
[9] Univ Texas MD Anderson Canc Ctr, Div Canc Med, Houston, TX 77030 USA
关键词
EXTRACELLULAR-MATRIX PROTEINS; LET-7; MICRORNA; HEPATOCELLULAR-CARCINOMA; BETA-CATENIN; STEM-CELLS; CYCLIN D1; C-ELEGANS; LIN-28; IDENTIFICATION; EXPRESSION;
D O I
10.1158/0008-5472.CAN-10-4637
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
LIN28B is a homologue of LIN28 that induces pluripotency when expressed in conjunction with OCT4, SOX2, and KLF4 in somatic fibroblasts. LIN28B represses biogenesis of let-7 microRNAs and is implicated in both development and tumorigenesis. Recently, we have determined that LIN28B overexpression occurs in colon tumors. We conducted a comprehensive analysis of LIN28B protein expression in human colon adenocarcinomas. We found that LIN28B overexpression correlates with reduced patient survival and increased probability of tumor recurrence. To elucidate tumorigenic functions of LIN28B, we constitutively expressed LIN28B in colon cancer cells and evaluated tumor formation in vivo. Tumors with constitutive LIN28B expression exhibit increased expression of colonic stem cell markers LGR5 and PROM1, mucinous differentiation, and metastasis. Together, our findings point to a function for LIN28B in promoting colon tumor pathogenesis, especially metastasis. Cancer Res; 71(12); 4260-8. (C)2011 AACR.
引用
收藏
页码:4260 / 4268
页数:9
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