BTN3A3 inhibits clear cell renal cell carcinoma progression by regulating the ROS/MAPK pathway via interacting with

Zhangyun Li1, Mengmeng Zhang1, Sihan Chen2

  • 1School of Life Science, Jiangsu Normal University, Xuzhou, Jiangsu, China.

Cellular Signalling
|October 8, 2023
PubMed

Insights

High levels of Butyrophilin subfamily 3 member A3 (BTN3A3) correlate with longer survival in clear cell renal cell carcinoma (ccRCC). BTN3A3 inhibits ccRCC progression by interacting with RPS3A and modulating MAPK signaling via reactive oxygen species (ROS).

Area of Science:

  • Oncology
  • Molecular Biology
  • Immunology

Background:

  • Butyrophilin subfamily 3 member A3 (BTN3A3) is an immunoglobulin superfamily member with tumor suppressor functions.
  • Clear cell renal cell carcinoma (ccRCC) is a significant malignancy where prognostic markers are crucial.

Purpose of the Study:

  • To investigate the role of BTN3A3 in ccRCC progression.
  • To identify interacting partners of BTN3A3 and elucidate its molecular mechanisms in ccRCC.

Main Methods:

  • Immunoprecipitation followed by mass spectrometry to identify BTN3A3 interacting proteins.
  • Cell proliferation, migration, and invasion assays.
  • Analysis of mitochondrial function, reactive oxygen species (ROS) levels, and MAPK signaling pathway activation.
  • RNA-Seq and immunoblotting.

Main Results:

  • High BTN3A3 expression is associated with longer survival in ccRCC patients.
  • BTN3A3 directly binds to RPS3A, and this interaction inhibits ccRCC cell proliferation, migration, and invasion.
  • BTN3A3 and RPS3A co-expression increases cellular oxygen consumption rate (OCR) and ROS levels.
  • BTN3A3 negatively regulates MAPK pathway activation, suggesting a role in ccRCC progression via ROS and MAPK signaling.

Conclusions:

  • BTN3A3 acts as a tumor suppressor in ccRCC by inhibiting cell proliferation, migration, and invasion.
  • The BTN3A3/RPS3A complex regulates ccRCC progression, potentially through modulation of ROS and MAPK pathways.
  • BTN3A3 shows promise as a prognostic marker and a therapeutic target for ccRCC.

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