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SCI 발표논문

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Pancreas. 2012;41(7):1048-57.

Enhanced antitumor effect of combination therapy with gemcitabine and guggulsterone in pancreatic cancer.

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제1저자 안동원/서정균 · 교신저자 이상협

소속 (1)
  1. Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea.

Abstract

OBJECTIVES Guggulsterone is a dietary plant sterone possessing therapeutic potential against cancers. However, the antitumor effect of this natural compound on pancreatic cancer has not been determined yet. This study was designed to investigate the therapeutic efficacy of guggulsterone in pancreatic cancer.

METHODS In this study, we examined the effect of guggulsterone on cell proliferation and apoptosis in pancreatic cancer cell lines, and then, we investigated the mechanisms responsible for the effect of guggulsterone. Finally, we investigated whether the combination of guggulsterone and gemcitabine had an additional therapeutic effect compared to gemcitabine single regimen in pancreatic cancer cell lines (in vitro) and in a xenograft model using nude mice (in vivo).

RESULTS In vitro, the combination treatment resulted in more growth inhibition and apoptosis through the down-regulation of nuclear factor κB activity with suppression of Akt and BcL-2 and through the activation of c-Jun NH(2)-terminal kinase and Bax in pancreatic cancer cell lines. In vivo, the combination therapy augmented tumor growth inhibition through the same mechanisms in tumor tissue.

CONCLUSIONS The combination of guggulsterone to gemcitabine enhanced antitumor efficacy through apoptosis induction by suppressing Akt and nuclear factor κB activity and by modulating apoptosis-related protein expression in pancreatic cancer.

그 밖의 정보
출판 형태
Journal Article, Research Support, Non-U.S. Gov't
저널
Pancreas · eISSN 1536-4828
MeSH
Animals · Antimetabolites, Antineoplastic · Antineoplastic Agents, Phytogenic · Antineoplastic Combined Chemotherapy Protocols / pharmacology / therapeutic use · Apoptosis / drug effects · Cell Line, Tumor · Cell Proliferation / drug effects · DNA / metabolism · Deoxycytidine / administration & dosage / analogs & derivatives · Drug Synergism · Humans · In Situ Nick-End Labeling · Male · Mice · Mice, Inbred BALB C · Mice, Nude · NF-kappa B / antagonists & inhibitors / metabolism · Oncogene Protein v-akt / antagonists & inhibitors · Pancreatic Neoplasms / drug therapy · Pregnenediones / administration & dosage · Xenograft Model Antitumor Assays · Gemcitabine
Substances
Antimetabolites, Antineoplastic · Antineoplastic Agents, Phytogenic · NF-kappa B · Pregnenediones · Deoxycytidine · DNA · pregna-4,17-diene-3,16-dione · Oncogene Protein v-akt · Gemcitabine