Evidence map›Paper›PMID 40640144›Full record

ArticleCell death discovery2025

The transcriptomic fingerprint of cancer response to Tumor Treating Fields (TTFields).

Kerem Wainer-Katsir, Adi Haber, Hila Fishman, Lianghao Ding, Michael D Story, Renfei Du, Ulf D Kahlert, Laura Mannarino, Federica Mirimao, Monica Lupi and 11 more

Abstract read
In one paragraph

Article in Cell death discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

21 authors.

Kerem Wainer-Katsir *Novocure LTD, Haifa, Israel.ORCID http://orcid.org/0009-0004-5634-8978
Adi Haber *Novocure LTD, Haifa, Israel.
Hila FishmanNovocure LTD, Haifa, Israel.
Lianghao DingDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Michael D StoryDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Renfei DuClinic for Neurosurgery, Heinrich-Heine University, Duesseldorf, Germany.
Ulf D KahlertMolecular and Experimental Surgery, University Clinic for General-, Visceral-, Vascular- and Trans-Plantation Surgery, Medical Faculty and University Hospital Magdeburg, Otto-von Guericke University, Magdeburg, Germany.ORCID http://orcid.org/0000-0002-6021-1841
Laura MannarinoLaboratory of Cancer Pharmacology, IRCCS Humanitas Research Hospital, Milano, Italy.
Federica MirimaoDepartment of Oncology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milano, Italy.
Monica LupiLaboratory of Cancer Pharmacology, IRCCS Humanitas Research Hospital, Milano, Italy.ORCID http://orcid.org/0000-0002-9835-7870
Maurizio D'IncalciLaboratory of Cancer Pharmacology, IRCCS Humanitas Research Hospital, Milano, Italy.ORCID http://orcid.org/0000-0001-8784-1360
Gitit Lavy-ShahafNovocure LTD, Haifa, Israel.
Hila EneNovocure LTD, Haifa, Israel.
Roni Frechtel-GerziNovocure LTD, Haifa, Israel.
Zeina DrawshyNovocure LTD, Haifa, Israel.
Antonia Martinez-CondeNovocure LTD, Haifa, Israel.
Eyal Dor-OnNovocure LTD, Haifa, Israel.
Yaara PoratNovocure LTD, Haifa, Israel.
Moshe GiladiNovocure LTD, Haifa, Israel. mosheg@novocure.com.ORCID http://orcid.org/0000-0003-1489-4175
Uri WeinbergNovocure LTD, Haifa, Israel.
Yoram PaltiNovocure LTD, Haifa, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor Treating Fields (TTFields) therapy is an approved cancer treatment modality, based on non-invasive application of electric fields to the tumor region. Proteomic and cell biology methods revealed a versatile mechanism of action to be involved in the response to TTFields. In the current research we performed whole transcriptome analysis across tumor types to identify pan-cancer responses to TTFields. For this we collected samples from control and TTFields-treated human cancer cell lines of gastric cancer, pancreatic cancer, ovarian cancer, non-small cell lung carcinoma, pleural mesothelioma, and glioblastoma. The transcriptomic analysis supported previous reported effects: downregulation of pathways associated with cell cycle, cell growth, and proliferation; downregulation of DNA replication and the FA-BRCA DNA repair pathway; and upregulation of cellular responses to stress-senescence, autophagy, and apoptosis. Notably, previously unrecognized downstream effects of TTFields were revealed on cellular metabolism, with downregulation of protein and RNA metabolism, and upregulation of steroid biosynthesis. Additional DNA repair pathways were also found to be downregulated, including nucleotide excision repair, base excision repair, and mismatch repair. In conclusion, this study revealed similar response patterns to TTFields across different tumor types, re-enforcing some already pinpointed mechanisms, while revealing new mechanisms. Unlocking these new mechanisms may allow identification of potential new cancer treatments for application together with TTFields based on mechanistical compatibility.

Identifiers

PMID40640144
PMCPMC12246047

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.