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Cyclooxygenase-2 mediated synergistic effect of ursolic acid in combination with paclitaxel against human gastric carcinoma.
Xu, Xian; Zhu, Guo-Qin; Zhang, Kai; Zhou, Yi-Chan; Li, Xiao-Lin; Xu, Wei; Zhang, Hao; Shao, Yun; Zhang, Zhen-Yu; Sun, Wei-Hao.
Afiliação
  • Xu X; Department of Geriatric Gastroenterology, The First Affiliated Hospital to Nanjing Medical University, Nanjing 210029, China.
  • Zhu GQ; Department of Gastroenterology, Nanjing First Hospital, Nanjing Medical University, Nanjing 210006, China.
  • Zhang K; Department of Geriatric Gastroenterology, The First Affiliated Hospital to Nanjing Medical University, Nanjing 210029, China.
  • Zhou YC; Department of Geriatric, Huadong Hospital Affiliated to Fudan University, Shanghai 200040, China.
  • Li XL; Department of Geriatric Gastroenterology, The First Affiliated Hospital to Nanjing Medical University, Nanjing 210029, China.
  • Xu W; Department of Geriatric Gastroenterology, The First Affiliated Hospital to Nanjing Medical University, Nanjing 210029, China.
  • Zhang H; Department of Geriatric Gastroenterology, The First Affiliated Hospital to Nanjing Medical University, Nanjing 210029, China.
  • Shao Y; Department of Geriatric Gastroenterology, The First Affiliated Hospital to Nanjing Medical University, Nanjing 210029, China.
  • Zhang ZY; Department of Geriatric Gastroenterology, The First Affiliated Hospital to Nanjing Medical University, Nanjing 210029, China.
  • Sun WH; Department of Gastroenterology, Nanjing First Hospital, Nanjing Medical University, Nanjing 210006, China.
Oncotarget ; 8(54): 92770-92777, 2017 Nov 03.
Article em En | MEDLINE | ID: mdl-29190954
ABSTRACT
Ursolic acid (UA) induces apoptosis in gastric cancer cells by inhibiting cyclooxygenase-2 (COX-2). Paclitaxel (PTX) is an important chemotherapy agent used to treat solid tumors. We evaluated the in vitro antitumor activity of UA in combination with PTX against gastric cancer cells and investigated the mechanisms underlying the combined effects. A cytotoxicity test and flow cytometry were utilized to study the effects of UA and PTX on proliferation and apoptosis, respectively. To further elucidate the mechanism, Western blot analysis was used to assess changes in the expression of a series of related proteins, including COX-2, proliferating cell nuclear antigen (PCNA), Bcl-2, and Bax. UA and PTX dose- and time-dependently inhibited BGC-823 and SGC-7901 gastric cancer cell proliferation. Combined delivery of UA and PTX synergistically reduced cell proliferation and induced apoptosis in these cells by lowering COX-2, PCNA, and Bcl-2 expression and by increasing Bax expression. These results indicate that the synergistic inhibition of proliferation and induction of apoptosis by UA and PTX may be induced by reducing COX-2 expression in gastric cancer cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Oncotarget Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Oncotarget Ano de publicação: 2017 Tipo de documento: Article