Evidence map›Paper›PMID 41588903›Full record

ReviewAnti-cancer agents in medicinal chemistry2026

Comprehensive Biochemical Insights into Prostate-Specific Antigen: From Biomarker to Functional Mediator in Prostate Cancer Pathophysiology.

Laxmidhar Das

Abstract readReview
PubMed Publisher
In one paragraph

Review in Anti-cancer agents in medicinal chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Laxmidhar DasCenter for Biotechnology, Siksha 'O' Anusandhan (Deemed to be University), Bhubaneswar, 751003, Odisha, India.ORCID 0000-0003-2690-5409

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate-Specific Antigen (PSA) is a glycoprotein produced in the prostate and is widely used as a biomarker for the diagnosis of prostate cancer (PCa). Although elevated PSA levels are often associated with PCa, several noncancerous conditions can also lead to increased PSA. In addition to total PSA, various PSA isoforms are detectable in the blood of patients, and their levels may differ depending on the underlying pathophysiological condition, whether benign or malignant. Measuring serum PSA levels alone is not sufficient to detect PCa, leading to widespread overdiagnosis and overtreatment. Therefore, comprehensive biochemical insights into PSA and its isoforms, of normal, benign, and malignant origin, may improve PSA assays for PCa diagnosis. Apart from its role as a biomarker, PSA plays multiple roles in the pathophysiology of PCa by activating the Epithelial-Mesenchymal Transition (EMT) and promoting tumor progression, as well as regulating the invasion and metastasis of PCa cells. In PCa, elevated PSA levels are associated with immunosuppression, antiapoptotic properties, and inhibition of angiogenesis. A comprehensive review of numerous important research findings on PSA and its isoforms was conducted to elucidate the role of PSA as a biomarker and functional mediator in PCa pathophysiology. Thus, the use of PSA as a biomarker for the diagnosis of PCa can minimize unnecessary and inappropriate biopsies, identify suitable patients for prostate biopsy, ensure early diagnosis, and initiate treatment at an early stage of PCa. Furthermore, the role of PSA as a functional mediator will enable us to study the pathophysiology of patients with prostate cancer (PCa).

Indexed as

Biomarkers, TumorProstate-Specific AntigenProstatic NeoplasmsHumansMaleBiomarkers, TumorProstate-Specific Antigenbenign prostatic hyperplasiabiomarkerdiagnosisfunctions of PSAisoforms of PSAProstate cancerprostate-specific antigen

Identifiers

PMID41588903

What OpenQuestion holds

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Registered trials

None linked

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 OpenQuestion graph.