4.7 Article

Modified Bu-zhong-yi-qi decoction synergies with 5 fluorouracile to inhibits gastric cancer progress via PD-1/PD-L1-dependent T cell immunization

期刊

PHARMACOLOGICAL RESEARCH
卷 152, 期 -, 页码 -

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phrs.2019.104623

关键词

Bu-zhong-yi-qi decoction; T cell; Gastric cancer; PD-1; PD-L1

资金

  1. National Natural Science Foundation of China [81973609, 81973782, 81473605, 81704031]
  2. Jiangsu Provincial Medical Youth Talent [QNRC2016641]
  3. 333 Project of Jiangsu Province [LGY2018065]
  4. Jiangsu Provincial Hospital of Traditional Chinese Medicine Academic Talent Program [Y2018RC33]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  6. Open Projects of the Discipline of Chinese Medicine of Nanjing University of Chinese Medicine -Subject of Academic priority discipline of Jiangsu Higher Education Institutions [ZYX03KF019, ZYX03KF021, ZYX03KF029]
  7. Postgraduate Research & Practice Innovation Program of Jiangsu Province [SJCX17-0395]
  8. Science and Technology Program for Social Development of Jiangsu Province, China [BE2019771]

向作者/读者索取更多资源

Gastric cancer remains the second most common tumor in China. Modified-Bu-zhong-yi-qi decoction (mBYD) as an adjuvant therapy for gastric cancer patients after chemotherapy could significantly prolong the survival time of patients. However, the potential anticancer mechanism for mBYD has not been well characterized. Here, we conducted a comprehensive study of mBYD on a gastric cancer xenograft model with MFC cells in 615 mice and patients. Our results showed that the survival times of the 5-FU + mBYD and mBYD groups were significantly longer than that of the control group. Moreover, the 5-FU + mBYD group had a longer survival time than the 5-FU group. Flow cytometry revealed that the value of CD4(+)/CD8(+) in the mBYD group increased and that the proportions of CD8(+)PD-1(+) T cells and PD-1(+)Treg cells were decreased when compared to the control group. Compared with the 5-FU group, CD8(+)PD-1(+) T cells and Treg cells were both decreased when 5-FU was combined with mBYD. Further analysis showed that mBYD inhibited PD-L1 expression by the PI3K/AKT pathway in gastric cancer. An in vitro study also showed that mBYD directly promoted the proliferation, activation and cytotoxicity of T lymphocytes. Meanwhile, mBYD reduced the upregulation of CD8(+)PD-1(+) T cells induced by chemotherapy in patients with gastric cancer. In conclusion, mBYD could modulate peripheral immunity and suppress the immune escape of tumors, which may be a promising therapy for gastric cancer.

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