Antitumor effects of herbal mixture extract in the pancreatic adenocarcinoma cell line PANC1
- Authors
- Pak, Pyo June; Kang, Beob Hwa; Park, Sung Hyo; Sung, Ji Hyun; Joo, Yong Hoon; Jung, Seung Hyun; Chung, Namhyun
- Issue Date
- 11월-2016
- Publisher
- SPANDIDOS PUBL LTD
- Keywords
- cancer stem cell; pancreatic cancer; traditional medicinal herb; side population; xenograft model
- Citation
- ONCOLOGY REPORTS, v.36, no.5, pp.2875 - 2883
- Indexed
- SCIE
SCOPUS
- Journal Title
- ONCOLOGY REPORTS
- Volume
- 36
- Number
- 5
- Start Page
- 2875
- End Page
- 2883
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/86992
- DOI
- 10.3892/or.2016.5067
- ISSN
- 1021-335X
- Abstract
- A recent study showned that complementary medicine is gradually gaining wide acceptance. In the present study, the herbal mixture extract (H3) composed of 3 oriental herbal plants was investigated for anticancer activity in vitro and in vivo. H3 inhibited PANC1 cell growth by promoting G0/G1 arrest (11% increase) and apoptotic cell death (9% increase). H3 also suppressed stem cell-like side population cells (4% decrease) and migration activity (24% decrease). In contrast, gemcitabine decreased side population cells and migration activity by 3 and 11%, respectively. These effects of H3 and gemcitabine were further studied by examining the expression of apoptosis-associated genes (CXCR4, JAK2 and XIAP) and stem cell-associated genes (ABCG2, POU5F1 and SOX2). We also found that H3 suppressed tumor growth by 46% in a PANC1-xenograft model, while gemcitabine caused a 36% decrease. The antitumor effects of H3 were confirmed by western blot analysis for COX-2 and cytochrome c expression. Furthermore, necrotic cell death and erythrocyte-containing cavities were detected in tumor tissue by hematoxylin and eosin (H&E) staining. Notably, the combinatorial therapy (H3 and gemcitabine) increased tumor growth compared to that in the control. In conclusion, the present study shows that H3 has promise as a therapeutic agent against pancreatic cancer and its cancer stem cells.
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Collections - Graduate School > Department of Biosystems and Biotechnology > 1. Journal Articles
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