Evidence map›Paper›PMID 42363281›Full record

ArticleCell & bioscience2026

The TSPY gene and the loss of Y chromosome predisposition to cancers.

Yun-Fai Chris Lau

Abstract readLetter
In one paragraph

Article in Cell & bioscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Yun-Fai Chris LauDepartment of Medicine, San Francisco VA Health Care System, VA Medical Center, 111C5, University of California, San Francisco, 4150 Clement Street, 94121, San Francisco, CA, USA. chris.lau@ucsf.edu.ORCID https://orcid.org/0000-0002-9119-7050

Funding

U.S. Department of Veterans Affairs 2I01BX004446
6 · The paper itself

Abstract

Mosaic loss of Y chromosome is a common genetic phenomenon in elderly men. It predisposes affected individuals to cancers, suggesting that genes on this male-specific chromosome contribute to the well-being of men. Currently, the putative gene(s) responsible for such cancer predisposition when lost is/are currently unknown. A recent study identified the testis-specific protein Y-encoded (TSPY) gene possesses significant immunogenicity, capable of eliciting significant immune responses against and eliminating positive tumor cells in a mouse model of liver cancer. TSPY is a male-specific cancer-testis antigen expressed in a wide variety of cancers but not normal somatic cells. It is an ampliconic gene constituting a majority (~ 42%) of all protein-coding genes on the human Y chromosome. TSPY is hypothesized to be a guardian gene for man, protecting man from cancer development. Its high copy-number of conserved functional units ensures that it is intrinsically activated in early/progenitor cancer cells, thereby eliciting robust immune responses, eliminating early tumor progenitor cells and preempting oncogenic progression and tumor development. Loss of TSPY gene cluster together with the loss of the entire Y chromosome in oncogenic progenitor/early tumor cells provide a favorable environment fostering oncogenic development, thereby predisposing elderly men to cancers.

Identifiers

PMID42363281
PMCPMC13307705

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.