Evidence map›Paper›PMID 29403306›Full record

ArticleCancer growth and metastasis2017

Upregulated Heat Shock Proteins After Hyperthermic Chemotherapy Point to Induced Cell Survival Mechanisms in Affected Tumor Cells From Peritoneal Carcinomatosis.

Tanja Grimmig, Eva-Maria Moll, Kerstin Kloos, Rebecca Thumm, Romana Moench, Simone Callies, Jennifer Kreckel, Malte Vetterlein, Joerg Pelz, Buelent Polat and 7 more

Open access · diamondAbstract read
In one paragraph

Article in Cancer growth and metastasis, 2017. 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
2.5field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  6. HYPER: pre-clinical device for spatially-confined magnetic particle hyperthermia.International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2023
    Article
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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

17 authors at 4 institutions in 2 countries.

Tanja GrimmigDepartment of Surgery I, Molecular Oncology and Immunology, University of Wuerzburg, Wuerzburg, Germany.
Eva-Maria MollDepartment of Surgery I, Molecular Oncology and Immunology, University of Wuerzburg, Wuerzburg, Germany.
Kerstin KloosDepartment of Surgery I, Molecular Oncology and Immunology, University of Wuerzburg, Wuerzburg, Germany.
Rebecca ThummDepartment of Surgery I, Molecular Oncology and Immunology, University of Wuerzburg, Wuerzburg, Germany.
Romana MoenchDepartment of Surgery I, Molecular Oncology and Immunology, University of Wuerzburg, Wuerzburg, Germany.
Simone CalliesDepartment of Surgery I, Molecular Oncology and Immunology, University of Wuerzburg, Wuerzburg, Germany.
Jennifer KreckelDivision of Molecular Internal Medicine, Department of Internal Medicine II, University of Wuerzburg, Wuerzburg, Germany.
Malte VetterleinDepartment of Urology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Joerg PelzDepartment of Surgery I, University of Wuerzburg, Wuerzburg, Germany.
Buelent PolatDepartment of Radiation Oncology, University of Wuerzburg, Wuerzburg, Germany.
Sudipta TripathiTransplant Research Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Roberta RehderEvangelical Medical School, Faculty University of Parana, Curitiba, Brazil.
Carmen M RibasEvangelical Medical School, Faculty University of Parana, Curitiba, Brazil.
Anil ChandrakerTransplant Research Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Christoph-T GermerDepartment of Surgery I, University of Wuerzburg, Wuerzburg, Germany.
Ana Maria Waaga-GasserDepartment of Surgery I, Molecular Oncology and Immunology, University of Wuerzburg, Wuerzburg, Germany.
Martin GasserDepartment of Surgery I, University of Wuerzburg, Wuerzburg, Germany.
University of Würzburg · DEHarvard University · USBrigham and Women's Hospital · USUniversity Medical Center Hamburg-Eppendorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In patients with peritoneal carcinomatosis cytoreductive surgery combined with hyperthermic intraperitoneal chemotherapy (HIPEC) represents a promising treatment strategy. Here, we studied the role of hyperthermic chemotherapy on heat shock protein (HSP) expression and induction of tumor cell death and survival. HSP27, HSP70, and HSP90 combined with effects on tumor cell proliferation and chemosensitivity were analyzed in human colon cancer. Hyperthermic chemotherapy resulted in significant HSP27/HSP70 and HSP90 gene/protein overexpression in analyzed HT-29/SW480/SW620 colon cancer cells and peritoneal metastases from patients displaying amplified expression of proliferation markers, proliferating cell nuclear antigen and antiapoptotic protein Bcl-xL. Moreover, functionally increased chemoresistance against 5-fluorouracil/mitomycin C and oxaliplatin after hyperthermic chemotherapy points to induced survival mechanisms in cancer cells. In conclusion, the results indicate that intracellular HSP-associated antiapoptotic and proliferative effects after hyperthermic chemotherapy negatively influence beneficial effects of hyperthermic chemotherapy-induced cell death. Therefore, blocking HSPs could be a promising strategy to further improve the rate of tumor cell death and outcome of patients undergoing HIPEC therapy.

Indexed as

apoptosischemoresistanceHeat shock proteinshyperthermiahyperthermic intraperitoneal chemotherapyperitoneal carcinomatosis

Identifiers

PMID29403306
PMCPMC5791678
OpenAlexW2754298229

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LicenceCC BY
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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.