4.7 Article

XIAOPI formula promotes breast cancer chemosensitivity via inhibiting CXCL1/HMGB1-mediated autophagy

期刊

BIOMEDICINE & PHARMACOTHERAPY
卷 120, 期 -, 页码 -

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2019.109519

关键词

Breast cancer chemosensitivity; Autophagy; CXCL1/HMGB1 axis; XIAOPI formula

资金

  1. National Natural Science Foundation of China [81973526, 81573651, 81873306, 81703764, 81703749]
  2. Guangdong Science and Technology Department [2016A030306025]
  3. Guangdong High-level Personnel of Special Support Program [A1-3002-16-111-003]
  4. Department of Education of Guangdong Province [2018KZDXM022, A1-2606-19-111-009]
  5. Traditional Chinese Medicine Bureau of Guangdong Province [20181132, 20182044]
  6. Natural Science Foundation of Guangdong Province [2017A030310213, 2018A030310506]
  7. Science and Technology Planning Project of Guangdong Province [2017B030314166]
  8. Guangzhou Municipal Science and Technology Project [201904010407]
  9. Specific Research Fund for TCM Science and Technology of Guangdong provincial Hospital of Chinese Medicine [YN2018MJ07, YN2018QJ08]

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XIAOPI formula is a national approved drug prescribed to patients with high breast cancer risk. Previously we demonstrated that XIAOPI formula could inhibit breast cancer metastasis via suppressing CXCL1 expression, and postulated that autophagy in cancer might be one of its most core anti-cancer mechanisms. However, whether XIAOPI formula could be simultaneously applied with chemodrugs and their synergistic mechanisms are still remained unknown. In the present study, XIAOPI formula at non-cytotoxic doses could synergistically enhance the chemosensitivity of breast cancer cells MDA-MB-231 and MCF-7. We found that rapamycin-induced autophagy could reduce the chemosensitivity of breast cancer cells to XIAOPI formula, and the autophagy suppression and chemosensitizing activity of this formula was CXCL1-dependent. The evidence came from that XIAOPI formula was associated with a lower expression of CXCL1 combined with either rapamycin or taxol alone. Besides, the inhibitory effect of XIAOPI formula on the LC3-II and ABCG2 signals was weakened following CXCL1 over-expression, whereas P62 upregulation induced by XIAOPI formula was re-declined. A high throughput qPCR (HT-qPCR) assay identified HMGB1 as the main autophagic target of XIAOPI formula in chemosensitizing breast cancer. and furhter validation suggested XIAOPI formula exerted chemosensitivity mainly via CXCL1/HMGB1 autophagic axis. Finally, we generated both mice and zebrafish xenotransplantation models bearing MDA-MB-231 breast cancer cells, and found that XIAOPI formula safely enhanced in vivo taxol chemosensitivity on breast cancer. Taken together, XIAOPI formula is a potential adjuvant drug via inhibiting CXCL1/HMGB1-mediated autophagy for breast cancer treatment with good safety.

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