SPAG6 regulates cell proliferation and apoptosis via TGF-β/Smad signal pathway in adult B-cell acute lymphoblastic leukemia

Int J Hematol. 2024 Feb;119(2):119-129. doi: 10.1007/s12185-023-03684-x. Epub 2023 Dec 26.

Abstract

Adult B-cell acute lymphoblastic leukemia (B-ALL) prognosis remains unsatisfactory, and searching for new therapeutic targets is crucial for improving patient prognosis. Sperm-associated antigen 6 (SPAG6), a member of the cancer-testis antigen family, plays an important role in tumors, especially hematologic tumors; however, it is unknown whether SPAG6 plays a role in adult B-ALL. In this study, we demonstrated for the first time that SPAG6 expression was up-regulated in the bone marrow of adult B-ALL patients compared to healthy donors, and expression was significantly reduced in patients who achieved complete remission (CR) after treatment. In addition, patients with high SPAG6 expression were older (≥ 35 years; P = 0.015), had elevated white blood cell counts (WBC > 30 × 109/L; P = 0.021), and a low rate of CR (P = 0.036). We explored the SPAG6 effect on cell function by lentiviral transfection of adult B-ALL cell lines BALL-1 and NALM-6, and discovered that knocking down SPAG6 significantly inhibited cell proliferation and promoted apoptosis. We identified that SPAG6 knockdown might regulate cell proliferation and apoptosis via the transforming growth factor-β (TGF-β)/Smad signaling pathway.

Keywords: Adult B-cell acute lymphoblastic leukemia; Apoptosis; Proliferation; SPAG6; TGF-β/Smad.

MeSH terms

  • Adult
  • Apoptosis / genetics
  • Cell Proliferation
  • Humans
  • Male
  • Microtubule Proteins / metabolism
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma*
  • Signal Transduction
  • Transforming Growth Factor beta*

Substances

  • Transforming Growth Factor beta
  • SPAG6 protein, human
  • Microtubule Proteins