TY - JOUR
T1 - KH-Type Splicing Regulatory Protein Controls Colorectal Cancer Cell Growth and Modulates the Tumor Microenvironment
AU - Caiazza, Francesco
AU - Oficjalska, Katarzyna
AU - Tosetto, Miriam
AU - Phelan, James J.
AU - Noonan, Sinéad
AU - Martin, Petra
AU - Killick, Kate
AU - Breen, Laura
AU - O'Neill, Fiona
AU - Nolan, Blathnaid
AU - Furney, Simon
AU - Power, Robert
AU - Fennelly, David
AU - Craik, Charles S.
AU - O'Sullivan, Jacintha
AU - Sheahan, Kieran
AU - Doherty, Glen A.
AU - Ryan, Elizabeth J.
N1 - Publisher Copyright:
© 2019 American Society for Investigative Pathology
PY - 2019/10
Y1 - 2019/10
N2 - KH-type splicing regulatory protein (KHSRP) is a multifunctional nucleic acid binding protein implicated in key aspects of cancer cell biology: inflammation and cell-fate determination. However, the role KHSRP plays in colorectal cancer (CRC) tumorigenesis remains largely unknown. Using a combination of in silico analysis of large data sets, ex vivo analysis of protein expression in patients, and mechanistic studies using in vitro models of CRC, we investigated the oncogenic role of KHSRP. We demonstrated KHSRP expression in the epithelial and stromal compartments of both primary and metastatic tumors. Elevated expression was found in tumor versus matched normal tissue, and these findings were validated in larger independent cohorts in silico. KHSRP expression was a prognostic indicator of worse overall survival (hazard ratio, 3.74; 95% CI, 1.43–22.97; P = 0.0138). Mechanistic data in CRC cell line models supported a role of KHSRP in driving epithelial cell proliferation in both a primary and metastatic setting, through control of the G1/S transition. In addition, KHSRP promoted a proangiogenic extracellular environment by regulating the secretion of oncogenic proteins involved in diverse cellular processes, such as migration and response to cellular stress. Our study provides novel mechanistic insight into the tumor-promoting effects of KHSRP in CRC.
AB - KH-type splicing regulatory protein (KHSRP) is a multifunctional nucleic acid binding protein implicated in key aspects of cancer cell biology: inflammation and cell-fate determination. However, the role KHSRP plays in colorectal cancer (CRC) tumorigenesis remains largely unknown. Using a combination of in silico analysis of large data sets, ex vivo analysis of protein expression in patients, and mechanistic studies using in vitro models of CRC, we investigated the oncogenic role of KHSRP. We demonstrated KHSRP expression in the epithelial and stromal compartments of both primary and metastatic tumors. Elevated expression was found in tumor versus matched normal tissue, and these findings were validated in larger independent cohorts in silico. KHSRP expression was a prognostic indicator of worse overall survival (hazard ratio, 3.74; 95% CI, 1.43–22.97; P = 0.0138). Mechanistic data in CRC cell line models supported a role of KHSRP in driving epithelial cell proliferation in both a primary and metastatic setting, through control of the G1/S transition. In addition, KHSRP promoted a proangiogenic extracellular environment by regulating the secretion of oncogenic proteins involved in diverse cellular processes, such as migration and response to cellular stress. Our study provides novel mechanistic insight into the tumor-promoting effects of KHSRP in CRC.
UR - http://www.scopus.com/inward/record.url?scp=85072312571&partnerID=8YFLogxK
U2 - 10.1016/j.ajpath.2019.07.004
DO - 10.1016/j.ajpath.2019.07.004
M3 - Article
C2 - 31404541
AN - SCOPUS:85072312571
SN - 0002-9440
VL - 189
SP - 1916
EP - 1932
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 10
ER -