Evidence map›Paper›PMID 41651411›Full record

ReviewThe Journal of biological chemistry2026

TNF-alpha: Roles in pathogenesis and therapeutics in cancer.

Miriam Valenzuela Cardenas, Theodore Scott Nowicki

Abstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. 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

2 authors.

Miriam Valenzuela CardenasDivision of Pediatric Hematology-Oncology, Department of Pediatrics, University of California Los Angeles, Los Angeles, California, USA.
Theodore Scott NowickiDivision of Pediatric Hematology-Oncology, Department of Pediatrics, University of California Los Angeles, Los Angeles, California, USA; Department of Microbiology, Immunology, and Molecular Genetics, University of California Los Angeles, Los Angeles, California, USA; Jonsson Comprehensive Cancer Center, University of California Los Angeles, Los Angeles, California, USA; Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, University of California Los Angeles, Los Angeles, California, USA; Molecular Biology Institute, University of California Los Angeles, Los Angeles, California, USA. Electronic address: tnowicki@mednet.ucla.edu.

Funding

TNF-alpha-"armed" TCR vectors to enhance adoptive cell therapy for solid tumorsR37CA289813 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Theodore Scott Nowicki · 2025 to 2026
$1.3M
Functional epigenomics of transgenic cellular immunotherapies for cancerK08CA241088 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI NOWICKI, THEODORE SCOTT · 2021 to 2025
$909k
NCI NIH HHS K08 CA241088NCI NIH HHS R37 CA289813
6 · The paper itself

Abstract

Tumor necrosis factor alpha (TNF-α) is a pleiotropic cytokine that can both facilitate tumor progression and directly mediate tumor cell killing. This dual role creates a conundrum in which TNF can be either beneficial or detrimental for a tumor, depending on the context. Herein, we describe the history of the cytokine, the cases in which TNF-α has been considered as a cancer immunotherapy, and the toxicities that can manifest from its use. We also add context to its activity, particularly in T cells (via the engagement of TNF receptors) as well as the epigenetic and immunoregulatory pathways that are elicited. Furthermore, we highlight the fundamental differences in the transcriptional and translational regulation of this cytokine, which plays a significant role in the context of malignancy and potential success of immunotherapies. This review aims to provide insight and background on molecular switches, cellular context, and TNF receptor dynamics that determine the role of TNF-α as both tumor suppressor and promoter in different models, which is essential for deriving maximal benefit from TNF therapies.

Indexed as

NeoplasmsTumor Necrosis Factor-alphaAnimalsHumansImmunotherapyReceptors, Tumor Necrosis FactorReceptors, Tumor Necrosis FactorTumor Necrosis Factor-alphacancerinflammationsignalingT-cellsTNF-alpha

Identifiers

PMID41651411
PMCPMC12962152

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.