Evidence map›Paper›PMID 39068512›Full record

ReviewMolecular therapy : the journal of the American Society of Gene Therapy2024

Mapping the cancer surface proteome in search of target antigens for immunotherapy.

Francesco Di Meo, Brandon Kale, John M Koomen, Fabiana Perna

Abstract readReview
In one paragraph

Review in Molecular therapy : the journal of the American Society of Gene Therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Cancers · 2025
    Review
  12. Review
  13. Staying on target in gene and cell therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
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

4 authors.

Francesco Di MeoDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, Tampa, FL, USA.
Brandon KaleDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, Tampa, FL, USA.
John M KoomenDepartment of Molecular Oncology, Moffitt Cancer Center, Tampa, FL, USA.
Fabiana PernaDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, Tampa, FL, USA. Electronic address: fabiana.perna@moffitt.org.

Funding

Identifying cell surface targets for innovative immunotherapy of Multiple MyelomaR37CA276939 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI Fabiana Perna · 2024 to 2026
$1.7M
Alternatively spliced cell surface proteins as drivers of leukemogenesis and targets for immunotherapyR21CA280367 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI PERNA, FABIANA · 2023 to 2024
$491k
NCI NIH HHS R21 CA280367NCI NIH HHS R37 CA276939
6 · The paper itself

Abstract

Immune-based therapeutic interventions recognizing proteins localized on the cell surface of cancer cells are emerging as a promising cancer treatment. Antibody-based therapies and engineered T cells are now approved by the Food and Drug Administration to treat some malignancies. These therapies utilize a few cell surface proteins highly expressed on cancer cells to release the negative regulation of immune activation that limits antitumor responses (e.g., PD-1, PD-L1, CTLA4) or to redirect the T cell specificity toward blood cancer cells (e.g., CD19 and B cell maturation antigen). One limitation preventing broader application of these novel therapeutic strategies to all cancer types is the lack of suitable target antigens for all indications owing in part to the challenges in identifying such targets. Ideal target antigens are cell surface proteins highly expressed on malignant cells and absent in healthy tissues. Technological advances in mass spectrometry, enrichment protocols, and computational tools for cell surface protein isolation and annotation have recently enabled comprehensive analyses of the cancer cell surface proteome, from which novel immunotherapeutic target antigens may emerge. Here, we review the most recent progress in this field.

Indexed as

Antigens, NeoplasmImmunotherapyNeoplasmsProteomeAnimalsHumansMembrane ProteinsProteomicsAntigens, NeoplasmMembrane ProteinsProteomeantigen discoverycell surface proteinscomputational toolsimmunotherapymass spectrometry

Identifiers

PMID39068512
PMCPMC11403220

What OpenQuestion holds

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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.