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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