Exploration of SUSD3 in pan-cancer: studying its role, predictive analysis, and biological significance in various malignant tumors in humans

  • 0Department of Laboratory Medicine, The Affiliated Huai'an Hospital of Xuzhou Medical University, The Second People's Hospital of Huai'an, Huai'an, Jiangsu, China.

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Summary

This summary is machine-generated.

Sushi domain containing 3 (SUSD3) protein expression is linked to cancer progression and patient prognosis. Targeting SUSD3 offers a promising strategy for novel cancer therapies and diagnostics.

Area Of Science

  • Oncology
  • Immunology
  • Molecular Biology

Background

  • The SUSD3 protein, characterized by its Sushi domain, is implicated in cancer progression, with expression levels correlating to tumor advancement and patient outcomes.
  • Altered SUSD3 expression may serve as a predictive biomarker for cancer progression, and it is recognized as a novel susceptibility marker.
  • SUSD3 presents a promising target for antibody-based therapies, potentially aiding in the prevention, diagnosis, and treatment of breast cancer.

Purpose Of The Study

  • To investigate the role of SUSD3 protein in various cancers and its potential as a therapeutic target.
  • To analyze SUSD3 expression patterns in different tissues and cell types within the tumor microenvironment.
  • To explore the prognostic significance and predictive value of SUSD3 in cancer immunotherapy.

Main Methods

  • Utilized HPA, GeneMANIA, The Cancer Genome Atlas, TISCH, and STOmics DB for expression analysis and tissue distribution.
  • Assessed prognostic significance using univariate Cox regression and explored genomic alterations via cBioPortal.
  • Investigated immunotherapy response, biological pathways (GSEA/GSVA), drug targets (CellMiner, CTRP, GDSC), and performed molecular docking and in vitro knockdown experiments.

Main Results

  • SUSD3 expression variations correlate with prognosis across multiple cancer types and are predominantly found in monocytes/macrophages and CD4+ T cells within the tumor microenvironment.
  • A strong association exists between SUSD3 expression, cancer immunotherapy biomarkers, immune cell infiltration, and immunomodulatory factors.
  • SUSD3 knockdown in breast cancer cells significantly inhibited proliferation and migration, with selumetinib identified as a potential inhibitor via molecular docking.

Conclusions

  • The study establishes a foundation for understanding SUSD3's role in pan-carcinomas, highlighting its immune regulatory functions.
  • Findings offer novel perspectives and potential therapeutic targets for developing innovative cancer treatment strategies.
  • SUSD3's involvement in cancer progression and its interaction with the immune system underscore its potential as a target for novel therapies.