Evidence map›Paper›PMID 33537086›Full record

ReviewTheranostics2021

Semaphorins as emerging clinical biomarkers and therapeutic targets in cancer.

Roberta Mastrantonio, Hua You, Luca Tamagnone

Open access · goldAbstract readReview
In one paragraph

Review in Theranostics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
4.4field-weighted citation impact, top 4% of its field
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

46 citing papers in PubMed, 60 citations in OpenAlex.

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  5. Advances in semaphorin 3B research in tumors (Review).Molecular and clinical oncology · 2026
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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

3 authors at 3 institutions in 2 countries.

Roberta MastrantonioUniversità Cattolica del Sacro Cuore, Rome, Italy.
Hua YouAffiliated Cancer Hospital & Institute of Guangzhou Medical University, China.
Luca TamagnoneUniversità Cattolica del Sacro Cuore, Rome, Italy.
Agostino Gemelli University Polyclinic · ITGuangzhou Medical University · CNUniversità Cattolica del Sacro Cuore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Semaphorins are a large family of developmental regulatory signals, characterized by aberrant expression in human cancers. These molecules crucially control cell-cell communication, cell migration, invasion and metastasis, tumor angiogenesis, inflammatory and anti-cancer immune responses. Semaphorins comprise secreted and cell surface-exposed molecules and their receptors are mainly found in the Plexin and Neuropilin families, which are further implicated in a signaling network controlling the tumor microenvironment. Accumulating evidence indicates that semaphorins may be considered as novel clinical biomarkers for cancer, especially for the prediction of patient survival and responsiveness to therapy. Moreover, preclinical experimental studies have demonstrated that targeting semaphorin signaling can interfere with tumor growth and/or metastatic dissemination, suggesting their relevance as novel therapeutic targets in cancer; this has also prompted the development of semaphorin-interfering molecules for application in the clinic. Here we will survey, in diverse human cancers, the current knowledge about the relevance of semaphorin family members, and conceptualize potential lines of future research development in this field.

Indexed as

AnimalsAntineoplastic AgentsBiomarkers, TumorCell Adhesion MoleculesCell CommunicationCell MovementGene Expression Regulation, NeoplasticHumansNeoplasm MetastasisNeoplasmsNeovascularization, PathologicNerve Tissue ProteinsNeuropilinsPrognosisSemaphorinsSignal TransductionAntineoplastic AgentsBiomarkers, TumorCell Adhesion MoleculesNerve Tissue ProteinsNeuropilinsplexinSemaphorinscancerneuropilinplexinpredictive biomarkersprognostic biomarkerssemaphorintherapy

Identifiers

PMID33537086
PMCPMC7847692
OpenAlexW3127306899

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.