Pyridoxal kinase and poly(ADP-ribose) affect the immune microenvironment of locally advanced cancers.
Adrien JosephJuncheng PanJudith MichelsGuido KroemerMaria CastedoPublished in: Oncoimmunology (2021)
Malignant cells adapt to the hostile tumor microenvironment by escaping from, or actively suppressing, anticancer immune responses. In the past, we reported that reduced synthesis of active vitamin B6 (due to downregulation of pyridoxal kinase) or overactivation of poly(ADP-ribose) polymerase confers resistance to chemotherapy with cisplatin. Recently, we found that these prognostically adverse alterations in oncometabolism also correlate with the rarefaction of immune effectors in the tumor bed.
Keyphrases
- locally advanced
- immune response
- induced apoptosis
- signaling pathway
- rectal cancer
- neoadjuvant chemotherapy
- squamous cell carcinoma
- protein kinase
- cell cycle arrest
- tyrosine kinase
- phase ii study
- radiation therapy
- stem cells
- cell proliferation
- toll like receptor
- pi k akt
- clinical trial
- oxidative stress
- type iii
- study protocol
- adverse drug
- lymph node