Evidence map›Paper›PMID 41930712›Full record

ReviewTranslational oncology2026

Small but mighty: Peptides as next-generation immunotargeting agents in gynecological cancers.

Pankaj Garg, Madhu Krishna, Sharad S Singhal

Abstract readReview
In one paragraph

Review in Translational oncology, 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

3 authors.

Pankaj GargDepartment of Chemistry, GLA University, NH-19, Mathura-Delhi Road, Mathura, Uttar Pradesh, 281406, India.
Madhu KrishnaDepartment of Medical Oncology and Therapeutic Research, Beckman Research Institute of City of Hope, 1500 E Duarte Road, Duarte, CA, 91010, USA.
Sharad S SinghalDepartment of Medical Oncology and Therapeutic Research, Beckman Research Institute of City of Hope, 1500 E Duarte Road, Duarte, CA, 91010, USA. Electronic address: ssinghal@coh.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The most common cancers in women, ovarian, cervical and endometrial, are still a significant cause of cancer-related illness and death around the world. Success with the newest immunotherapy can only be achieved when the treatment targets the tumor accurately. Although monoclonal antibodies, aptamers and antisense oligonucleotides are traditionally used in immunotargeting, they face challenges related to bulkiness, their price, immune response and reaching tumors. For these reasons, peptides are now considered important next-generation substances for immunotargeting. This review describes how peptides are becoming increasingly significant in gynecological oncology through their application in drug targeting, imaging cancer, and making vaccines. Findings on how peptide targeting systems measure up to other approaches and some recent advances in designing peptide-drug conjugates, receptor-targeting therapies, and CAR-T therapies are discussed. This review also discuss about how peptides are stable, how to deliver them selectively and how artificial intelligence supports better peptide designing. With the development of precision medicine, the use of peptide-based immunotargeting can greatly improve both the success and safety of treatments for cancer of the uterus and ovaries.

Indexed as

Gynecological cancersImmunotargeting agentsPeptide based cancer vaccinesPeptide-drug conjugatesTargeted drug deliveryTumor-specific ligands

Identifiers

PMID41930712
PMCPMC13087701

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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 OpenQuestion graph.