Evidence map›Paper›PMID 29311642›Full record

ArticleOncogene2018

HSP90 inhibition alters the chemotherapy-driven rearrangement of the oncogenic secretome.

Simona di Martino, Carla Azzurra Amoreo, Barbara Nuvoli, Rossella Galati, Sabrina Strano, Francesco Facciolo, Gabriele Alessandrini, Harvey I Pass, Gennaro Ciliberto, Giovanni Blandino and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  8. Heat Shock Protein 90 as Therapeutic Target for CVDs and Heart Ageing.International journal of molecular sciences · 2022
    Review
  9. Profile of soluble factors in pleural effusions predict prognosis in mesothelioma.Cancer biomarkers : section A of Disease markers · 2022
    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

12 authors at 4 institutions in 5 countries.

Simona di MartinoOncogenomic and Epigenetic Unit Regina Elena National Cancer Institute, Rome, Italy.
Carla Azzurra AmoreoDepartment of Pathology Regina Elena National Cancer Institute, Rome, Italy.
Barbara NuvoliPreclinical Models and New Therapeutic Agents Unit, Regina Elena National Cancer Institute, Rome, Italy.
Rossella GalatiPreclinical Models and New Therapeutic Agents Unit, Regina Elena National Cancer Institute, Rome, Italy.
Sabrina StranoMolecular Chemoprevention Unit, Regina Elena National Cancer Institute, Rome, Italy.
Francesco FaccioloDepartment of Thoracic Surgery, Regina Elena National Cancer Institute, Rome, Italy.
Gabriele AlessandriniDepartment of Thoracic Surgery, Regina Elena National Cancer Institute, Rome, Italy.
Harvey I PassNew York University School of Medicine, Department of Cardiothoracic Surgery, New York, NY, USA.
Gennaro CilibertoScientific Direction, Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0003-2851-8605
Giovanni BlandinoOncogenomic and Epigenetic Unit Regina Elena National Cancer Institute, Rome, Italy.
Ruggero De MariaScientific Direction, Regina Elena National Cancer Institute, Rome, Italy. demariaruggero@gmail.com.
Mario CioceOncogenomic and Epigenetic Unit Regina Elena National Cancer Institute, Rome, Italy. mariocioce@gmail.com.
McMaster University · CAAgostino Gemelli University Polyclinic · ITNational Cancer Institute · MYNew York University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adaptive resistance to therapy is a hallmark of cancer progression. To date, it is not entirely clear how microenvironmental stimuli would mediate emergence of therapy-resistant cell subpopulations, although a rearrangement of the cancer cell secretome following therapy-induced stress can be pivotal for such a process. Here, by using the highly chemoresistant malignant pleural mesothelioma (MPM) as an experimental model, we unveiled a key contribution of the chaperone HSP90 at assisting a chemotherapy-instigated Senescence-Associated-Secretory-Phenotype (SASP). Thus, administration of a clinical trial grade, HSP90, inhibitor blunted the release of several cytokines by the chemotherapy-treated MPM cells, including interleukin (IL)-8. Reduction of IL-8 levels hampered the FAK-AKT signaling and inhibited 3D growth and migration. This correlated with downregulation of key EMT and chemoresistance genes and affected the survival of chemoresistant ALDH

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsCell Line, TumorCellular SenescenceCisplatinDrug Resistance, NeoplasmHSP90 Heat-Shock ProteinsHumansLung NeoplasmsMaleMesotheliomaMesothelioma, MalignantMiceMice, Inbred NODMice, SCIDPemetrexedCisplatinHSP90 Heat-Shock ProteinsPemetrexedSTA 9090Triazoles

Identifiers

PMID29311642
OpenAlexW2782314122

What Socratic holds

Textmetadata
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.