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PMID: 17729412 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Elucidation of the relationship of BNIP3 expression to gemcitabine chemosensitivity and prognosis.

World journal of gastroenterology ·Vol. 13 ·No. 34 ·2007-09-14 ·Pages 4593-7

Ishida M, Sunamura M, Furukawa T, Akada M, Fujimura H, Shibuya E, Egawa S, Unno M, Horii A

Abstract

To evaluate the significance of BNIP3 in the pathogenesis of pancreatic cancer, we analyzed the relationship between the expression of BNIP3 and survival rate of the patients with pancreatic cancer, or chemosensitivities in pancreatic cancer cell lines, particularly for gemcitabine, the first-line anti-tumor drug for pancreatic cancer. To compare the expression level of BNIP3 with the resistance to gemcitabine, eight pancreatic cancer cell lines were subjected to gemcitabine treatment and the quantitative real-time RT-PCR method was used to evaluate BNIP3 expression. Immunohistochemical analysis was also performed using 22 pancreatic cancer specimens to study relationship between BNIP3 expression and survival rate. Although no significantly positive association between BNIP3 mRNA level and gemcitabine chemosensitivity was observed, pancreatic cancer cell lines that were sensitive to gemcitabine treatment tended to show high levels of BNIP3 expression. The converse, an absence of BNIP3 expression, was not correlated with gemcitabine resistance. We further compared the BNIP3 expression profiles of resected primary pancreatic cancer specimens with the prognosis of the patients, and found a tendency of favorable prognosis and low BNIP3 expression. High levels of BNIP3 expression cannot be used as one of the predicting factors for gemcitabine chemosensitivity, and some yet to be known factors will have to fill the gap for the accurate prediction of pancreatic cancer chemosensitivity to gemcitabine. However, BNIP3 expression may have an impact on prediction of prognosis of patients with pancreatic cancer.

MeSH Terms
Antimetabolites, Antineoplastic/pharmacology,therapeutic use Cell Line, Tumor Cell Proliferation/drug effects Cell Survival/drug effects Deoxycytidine/analogs & derivatives,pharmacology,therapeutic use Dose-Response Relationship, Drug Drug Resistance, Neoplasm Female Gene Expression Regulation, Neoplastic Humans Inhibitory Concentration 50 Kaplan-Meier Estimate Male Membrane Proteins/genetics,metabolism Middle Aged Pancreatic Neoplasms/drug therapy,genetics,metabolism,mortality,pathology Prognosis Proto-Oncogene Proteins/genetics,metabolism RNA, Messenger/metabolism Treatment Outcome
Chemicals
Antimetabolites, Antineoplastic BNIP3 protein, human Membrane Proteins Proto-Oncogene Proteins RNA, Messenger Deoxycytidine gemcitabine
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Ishida Masaharu
Department of Molecular Pathology, Tohoku University School of Medicine, 2-1 Seiryo-machi, Sendai, Japan.
Sunamura Makoto
Furukawa Toru
Akada Masanori
Fujimura Hiroko
Shibuya Emiko
Egawa Shinichi
Unno Michiaki
Horii Akira
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Article Info
Journal
World journal of gastroenterology
Abbr.
World J Gastroenterol
ISSN
1007-9327
Published
2007-09-14
Pages
4593-7
Language
English
Region
United States
NLM ID
100883448
PMCID
PMC4611833
Subset
IM
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