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Vitamin B6 Competition in the Tumor Microenvironment Hampers Antitumor Functions of NK Cells.
He, Chunbo; Wang, Dezhen; Shukla, Surendra K; Hu, Tuo; Thakur, Ravi; Fu, Xiao; King, Ryan J; Kollala, Sai Sundeep; Attri, Kuldeep S; Murthy, Divya; Chaika, Nina V; Fujii, Yuki; Gonzalez, Daisy; Pacheco, Camila G; Qiu, Yudong; Singh, Pankaj K; Locasale, Jason W; Mehla, Kamiya.
Affiliation
  • He C; Department of Oncology Science, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
  • Wang D; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
  • Shukla SK; Department of Oncology Science, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
  • Hu T; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
  • Thakur R; Department of Oncology Science, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
  • Fu X; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
  • King RJ; Department of General Surgery, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
  • Kollala SS; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
  • Attri KS; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
  • Murthy D; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
  • Chaika NV; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
  • Fujii Y; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
  • Gonzalez D; Department of Oncology Science, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
  • Pacheco CG; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
  • Qiu Y; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
  • Singh PK; Department of General Surgery, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
  • Locasale JW; Department of Oncology Science, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
  • Mehla K; Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, Nebraska.
Cancer Discov ; 14(1): 176-193, 2024 01 12.
Article in En | MEDLINE | ID: mdl-37931287
Nutritional factors play crucial roles in immune responses. The tumor-caused nutritional deficiencies are known to affect antitumor immunity. Here, we demonstrate that pancreatic ductal adenocarcinoma (PDAC) cells can suppress NK-cell cytotoxicity by restricting the accessibility of vitamin B6 (VB6). PDAC cells actively consume VB6 to support one-carbon metabolism, and thus tumor cell growth, causing VB6 deprivation in the tumor microenvironment. In comparison, NK cells require VB6 for intracellular glycogen breakdown, which serves as a critical energy source for NK-cell activation. VB6 supplementation in combination with one-carbon metabolism blockage effectively diminishes tumor burden in vivo. Our results expand the understanding of the critical role of micronutrients in regulating cancer progression and antitumor immunity, and open new avenues for developing novel therapeutic strategies against PDAC. SIGNIFICANCE: The nutrient competition among the different tumor microenvironment components drives tumor growth, immune tolerance, and therapeutic resistance. PDAC cells demand a high amount of VB6, thus competitively causing NK-cell dysfunction. Supplying VB6 with blocking VB6-dependent one-carbon metabolism amplifies the NK-cell antitumor immunity and inhibits tumor growth in PDAC models. This article is featured in Selected Articles from This Issue, p. 5.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Carcinoma, Pancreatic Ductal Limits: Humans Language: En Journal: Cancer Discov Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Carcinoma, Pancreatic Ductal Limits: Humans Language: En Journal: Cancer Discov Year: 2024 Document type: Article Country of publication: United States