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Sulforaphane impaired immune checkpoint blockade therapy through activating ΔNP63α/PD-L1 axis in gastric cancer.
Zhang, Qi; Yang, Chenying; Ma, Zhijian; Ye, Liangwen; Wu, Yunfeng; Zhong, Caiyun; Shi, Ye; Zhu, Mingming.
Afiliação
  • Zhang Q; Department of Public Health, School of Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
  • Yang C; Yinzhou Center for Disease Control and Prevention, Ningbo, China.
  • Ma Z; Department of Nutrition, School of Acupuncture and Tuina, Nanjing University of Chinese Medicine, Nanjing, China.
  • Ye L; The First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, China.
  • Wu Y; Department of Nutrition, School of Acupuncture and Tuina, Nanjing University of Chinese Medicine, Nanjing, China.
  • Zhong C; Department of Nutrition and Food Safety, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, China.
  • Shi Y; Department of Thoracic Surgery, Nanjing Chest Hospital, Affiliated Nanjing Brain Hospital, Nanjing Medical University, Nanjing, China.
  • Zhu M; Department of Nutrition, School of Acupuncture and Tuina, Nanjing University of Chinese Medicine, Nanjing, China.
Mol Carcinog ; 63(8): 1611-1620, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38780147
ABSTRACT
Sulforaphane (SFN) exerts anticancer effect on various cancers including gastric cancer. However, the regulatory effect of SFN on programmed death-ligand 1 (PD-L1) and checkpoint blockade therapy in gastric cancer have not been elucidated. Here we demonstrated that SFN suppressed gastric cancer cell growth both in vitro and in vivo study. SFN upregulated PD-L1 expression through activating ΔNP63α in gastric cancer cells. Further, we found that SFN impaired the anticancer effect of anti-PD-L1 monoclonal antibody (α-PD-L1 mab) on gastric cancer cells. These results uncover a novel PD-L1 regulatory mechanism and the double-edged role of SFN in gastric cancer intervention.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Sulfóxidos / Fatores de Transcrição / Isotiocianatos / Antígeno B7-H1 / Inibidores de Checkpoint Imunológico Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Gástricas / Sulfóxidos / Fatores de Transcrição / Isotiocianatos / Antígeno B7-H1 / Inibidores de Checkpoint Imunológico Idioma: En Ano de publicação: 2024 Tipo de documento: Article