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ID 118465
Title Alternative
LAMC2 promotes gemcitabine resistance in PDAC
Author
Okada, Yasuyuki Beckman Research Institute of City of Hope Comprehensive Cancer Center|Tokushima University Tokushima University Educator and Researcher Directory
Takahashi, Naoki Saitama Cancer Center
Goel, Ajay Beckman Research Institute of City of Hope Comprehensive Cancer Center
Keywords
LAMC2
pancreatic ductal adenocarcinoma
gemcitabine
EMT
ABC transporter
Content Type
Journal Article
Description
Pancreatic ductal adenocarcinoma (PDAC) is an aggressive disease with poor prognosis. Gemcitabine remains an effective option for the majority of PDAC patients. Unfortunately, currently no reliable prognostic and predictive biomarkers of therapeutic response are available for the patients with PDAC. Laminin γ2 (LAMC2) is overexpressed in several cancers, and its high expression facilitates cancer development and chemoresistance. However, its functional role in PDAC remains unclear, and a better understanding of this will likely help improve the prognosis of PDAC patients. This study aimed to elucidate the clinical and biological role of LAMC2 in PDAC. We first analyzed the expression levels of LAMC2 by real-time reverse transcription PCR in a cohort of 114 PDAC patients. Interestingly, higher expression of LAMC2 significantly correlated with poor survival in PDAC cohort. In addition, elevated LAMC2 expression served as a potential prognostic marker for survival. Subsequently, functional characterization for the role of LAMC2 in PDAC was performed by small interfering RNA (siRNA) knockdown in pancreatic cancer (PC) cell lines. Interestingly, inhibition of LAMC2 in PC cells enhanced the gemcitabine sensitivity and induction of apoptosis. Moreover, it inhibited colony formation ability, migration, and invasion potential. Furthermore, LAMC2 regulated the expression of epithelial-mesenchymal transition (EMT) phenotype. In addition, LAMC2 significantly correlated with genes associated with the expression of ATP-binding cassette (ABC) transporters in PC cells and PDAC patients. In conclusion, these results suggest that LAMC2 regulates gemcitabine sensitivity through EMT and ABC transporters in PDAC and may be a novel therapeutic target in PDAC patients.
Journal Title
Carcinogenesis
ISSN
14602180
01433334
NCID
AA12072343
AA00141799
Publisher
Oxford University Press
Volume
42
Issue
4
Start Page
546
End Page
556
Published Date
2021-02-24
Rights
This is a pre-copyedited, author-produced version of an article accepted for publication in Carcinogenesis following peer review. The version of record Yasuyuki Okada, Naoki Takahashi, Tetsuji Takayama, Ajay Goel, LAMC2 promotes cancer progression and gemcitabine resistance through modulation of EMT and ATP-binding cassette transporters in pancreatic ductal adenocarcinoma, Carcinogenesis, Volume 42, Issue 4, April 2021, Pages 546–556, is available online at: https://doi.org/10.1093/carcin/bgab011.
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DOI (Published Version)
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language
eng
TextVersion
Author
departments
University Hospital
Medical Sciences