Evidence mapPaperPMID 42578461Full record

ReviewCancer biology & therapy2026

The molecular mechanisms of platelets in tumor invasion and metastasis: a controversial role.

Amir Hossein Kheirkhah, Tahereh Zarei Taher, Zahra Khosrowpour, Omid Mahmoudian, Maria Kavianpour

Abstract readReview
In one paragraph

Review in Cancer biology & therapy, 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

5 authors.

Amir Hossein KheirkhahStudent Research Committee, Qom University of Medical Sciences, Qom, Iran.ORCID 0000-0002-7285-8554
Tahereh Zarei TaherStudent Research Committee, Qom University of Medical Sciences, Qom, Iran.ORCID 0000-0002-3428-0835
Zahra KhosrowpourDepartment of Pediatrics, University of Minnesota, Minneapolis, USA.ORCID 0000-0002-7243-7127
Omid MahmoudianFaculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran.ORCID 0009-0003-5776-2073
Maria KavianpourDepartment of Tissue Engineering and Applied Cell Sciences, Faculty of Medicine, Qom University of Medical Sciences, Qom, Iran.ORCID 0000-0002-8047-8754

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platelets, traditionally recognized for their role in hemostasis, are now understood to actively contribute to tumor progression, angiogenesis, and metastasis. Through dynamic bidirectional interactions with cancer cells, platelets undergo measurable alterations in count, mean platelet volume, and molecular cargo, including proteins and mRNAs, supporting their potential utility as liquid biopsy biomarkers for early cancer detection. Within the tumor microenvironment, platelets contribute to immune evasion, support tumor cell intravasation and extravasation, enhance the survival of circulating tumor cells, and promote neovascularization. In addition, they can physically shield malignant cells from immune surveillance, thereby increasing metastatic potential. Although context-specific anti-tumor effects have been reported, the predominant evidence supports a largely pro-tumorigenic and pro-metastatic role for platelets. Elucidating the molecular mechanisms underlying platelet-tumor interactions is therefore essential for improving cancer risk stratification, prognostic evaluation, and therapeutic development. This review summarizes current advances in platelet-derived biomarkers and discusses emerging therapeutic strategies targeting platelet-mediated pathways to suppress metastasis and improve clinical outcomes in cancer patients.

Indexed as

Blood PlateletsNeoplasmsAnimalsBiomarkers, TumorHumansNeoplasm InvasivenessNeoplasm MetastasisNeoplastic Cells, CirculatingNeovascularization, PathologicTumor MicroenvironmentBiomarkers, Tumorcancer progressioncirculating tumor cellsPlateletstargeted therapiestumor growthtumor metastasis

Identifiers

PMID42578461
PMCPMC13471101

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.