Evidence map›Paper›PMID 37598177›Full record

ArticleCell death & disease2023

HSF-1/miR-145-5p transcriptional axis enhances hyperthermic intraperitoneal chemotherapy efficacy on peritoneal ovarian carcinosis.

Silvia Di Agostino, Valeria Canu, Sara Donzelli, Claudio Pulito, Andrea Sacconi, Federica Ganci, Fabio Valenti, Frauke Goeman, Stefano Scalera, Francesca Rollo and 13 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. 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

23 authors at 4 institutions in 2 countries.

Silvia Di AgostinoDepartment of Health Sciences, Magna Græcia University of Catanzaro, 88100, Catanzaro, Italy.ORCID 0000-0003-3730-1125
Valeria CanuTranslational Oncology Research Unit, Department of Research, Diagnosis and Innovative Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Sara DonzelliTranslational Oncology Research Unit, Department of Research, Diagnosis and Innovative Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-8529-2895
Claudio PulitoTranslational Oncology Research Unit, Department of Research, Diagnosis and Innovative Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-0921-6962
Andrea SacconiClinical Trial Center, Biostatistics and Bioinformatics Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Federica GanciTranslational Oncology Research Unit, Department of Research, Diagnosis and Innovative Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Fabio ValentiTranslational Oncology Research Unit, Department of Research, Diagnosis and Innovative Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-1098-7705
Frauke GoemanSAFU Unit, Department of Research, Diagnosis and Innovative Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Stefano ScaleraSAFU Unit, Department of Research, Diagnosis and Innovative Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Francesca RolloDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0003-2724-872X
Anna BagnatoPreclinical Models and New Therapeutic Agents Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-7269-9522
Maria Grazia DiodoroDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Enrico VizzaGynecologic Oncology Unit, Department of Experimental Clinical Oncology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Mariantonia CarosiDepartment of Pathology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-6298-7168
Beatrice RufiniTranslational Oncology Research Unit, Department of Research, Diagnosis and Innovative Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Orietta FedericiDepartment of Digestive Surgery, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Manuel GiofrèDepartment of Digestive Surgery, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Fabio CarboniDepartment of Digestive Surgery, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Paola MutiDepartment of Biomedical, Surgical and Dental Sciences, University of Milan, Milan, Italy.
Gennaro CilibertoScientific Direction, IRCCS Regina Elena National Cancer Institute, 00144, Rome, Italy.ORCID 0000-0003-2851-8605
Sabrina StranoSAFU Unit, Department of Research, Diagnosis and Innovative Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Mario ValleDepartment of Digestive Surgery, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Giovanni BlandinoTranslational Oncology Research Unit, Department of Research, Diagnosis and Innovative Technologies, IRCCS Regina Elena National Cancer Institute, Rome, Italy. giovanni.blandino@ifo.it.ORCID 0000-0002-6970-2241
Istituti di Ricovero e Cura a Carattere Scientifico · ITMagna Graecia University · ITNational Cancer Institute · MYUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperthermic intraperitoneal administration of chemotherapy (HIPEC) increases local drug concentrations and reduces systemic side effects associated with prolonged adjuvant intraperitoneal exposure in patients affected by either peritoneal malignancies or metastatic diseases originating from gastric, colon, kidney, and ovarian primary tumors. Mechanistically, the anticancer effects of HIPEC have been poorly explored. Herein we documented that HIPEC treatment promoted miR-145-5p expression paired with a significant downregulation of its oncogenic target genes c-MYC, EGFR, OCT4, and MUC1 in a pilot cohort of patients with ovarian peritoneal metastatic lesions. RNA sequencing analyses of ovarian peritoneal metastatic nodules from HIPEC treated patients unveils HSF-1 as a transcriptional regulator factor of miR-145-5p expression. Notably, either depletion of HSF-1 expression or chemical inhibition of its transcriptional activity impaired miR-145-5p tumor suppressor activity and the response to cisplatin in ovarian cancer cell lines incubated at 42 °C. In aggregate, our findings highlight a novel transcriptional network involving HSF-1, miR145-5p, MYC, EGFR, MUC1, and OCT4 whose proper activity contributes to HIPEC anticancer efficacy in the treatment of ovarian metastatic peritoneal lesions.

Indexed as

MicroRNAsOvarian NeoplasmsCell LineErbB ReceptorsFemaleGenes, mycHeat Shock Transcription FactorsHumansHyperthermic Intraperitoneal ChemotherapyTranscription FactorsErbB ReceptorsHeat Shock Transcription FactorsMicroRNAsMIRN145 microRNA, humanTranscription Factors

Identifiers

PMID37598177
PMCPMC10439938
OpenAlexW4385999455

What Socratic 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 Socratic graph.