Evidence map›Paper›PMID 41613530›Full record

ArticleFrontiers in oncology2025

The expression of mercaptopyruvate sulfurtransferase serves as a potential biomarker for prognostic stratification and immunotherapy in certain cancers.

Boran Cui, Chenchen Xia, Li Yang, Xiaoyu Xi, Xinxin Gong, Yixi Liu, Cai Tian, Xiaoli Du, Jiexian Du, Zengfang Hao

Abstract read
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Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Boran Cui *Department of Gynecology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Chenchen Xia *Hebei Medical University, Shijiazhuang, Hebei, China.
Li Yang *Department of Gynecology, Xingtai Women and Children's Health, Xingtai, Hebei, China.
Xiaoyu XiDepartment of Gynecology, Peking University People's Hospital, Beijing, China.
Xinxin GongHebei North University, Zhangjiakou, Hebei, China.
Yixi LiuShandong First Medical University, Jinan, Shandong, China.
Cai TianDepartment of Gynecological Ultrasound, The First Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Xiaoli DuDepartment of Gynecology, Shijiazhuang Hospital of Traditional Chinese Medicine, Shijiazhuang, Hebei, China.
Jiexian DuDepartment of Gynecology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Zengfang HaoDepartment of Pathology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: 3 - Mercaptopyruvate Sulfurtransferase (3 - MST) is an enzyme encoded by the Mercaptopyruvate Sulfurtransferase (MPST) gene. The enzyme is associated with a variety of cancers such as lung adenocarcinoma. However, there is a lack of comprehensive pan-cancer analysis on the potential impact of MPST on cancer diagnosis, prognosis, and immune response. Methods: Based on data from The Cancer Genome Atlas and the Human Protein Atlas, we conducted a comprehensive bioinformatic analysis to investigate the oncogenic role of MPST. Immune-related characteristics and tumor microenvironment infiltration were assessed using TIMER2.0. Protein-protein interaction networks were constructed via STRING, while DNA methylation differences across cancers were analyzed with UALCAN. Further insights into genetic alterations and functional states at the single-cell level were obtained from cBioPortal and CancerSEA. Finally, clinical samples were collected and subjected to immunohistochemical staining to preliminarily validate the bioinformatic findings. Result: The research assessed the links between MPST levels and various cancer outcomes, genetic alterations, immune cell presence, and DNA methylation patterns. Single-cell sequencing was utilized to deepen our comprehension of its functional importance. Furthermore, the unique immunohistochemical profiling of MPST in patient tissue was confirmed. Significant expression differences between tumors and normal tissues in certain cancer types suggest a correlation between MPST expression and clinical outcomes. Furthermore, correlations exist between MPST expression levels in different immune cells and the tumor immune microenvironment. Our observations also indicate a role for MPST methylation, along with the advantageous effects of highly amplified mutations and deletions of the MPST gene. Discussion: Significantly, MPST shows potential for early cancer identification and as a predictive factor for various tumor forms.

Indexed as

immune infiltrationimmunohistochemistrymethylationMPSTpan-cancerprognosis

Identifiers

PMID41613530
PMCPMC12847049

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