Getting more bang for their buck: BCL2 inhibitors boost dendritic-cell function to enhance anti-cancer immune surveillance

J Transl Med. 2024 Mar 28;22(1):317. doi: 10.1186/s12967-024-04961-x.

Abstract

The anti-apoptotic BCL-2 protein family regulates cancer cell survival, thus it represents an important therapeutic target. Indeed, a drug class, called BH3-mimetics, have been developed to directly target BCL2 proteins and promote cancer cell death. Conventional wisdom suggests that the primary anti-cancer effect of BCL-2 inhibition is through induction of cancer cell death. However, a recent study by Zhao and colleagues describes that BCL-2 inhibition also enhances the function of classical dendritic cells, unleashing their role in immunosurveillance, promoting T cell immunity and tumour regression. Thus, inhibiting anti-apoptotic BCL-2 function may have a multi-pronged anti-tumour action.

Keywords: BCL-2; BH3 mimetics; DC maturation; Dendritic cells; Immune checkpoint inhibitors; Interferons; Venetoclax.

Publication types

  • Letter

MeSH terms

  • Antineoplastic Agents* / pharmacology
  • Antineoplastic Agents* / therapeutic use
  • Apoptosis
  • Apoptosis Regulatory Proteins / pharmacology
  • Apoptosis Regulatory Proteins / therapeutic use
  • Cell Line, Tumor
  • Humans
  • Neoplasms* / drug therapy
  • Neoplasms* / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / metabolism

Substances

  • Proto-Oncogene Proteins c-bcl-2
  • Antineoplastic Agents
  • Apoptosis Regulatory Proteins
  • BCL2 protein, human