Evidence map›Paper›PMID 32382008›Full record

ArticleCell death & disease2020

The USP10-HDAC6 axis confers cisplatin resistance in non-small cell lung cancer lacking wild-type p53.

Chen Hu, Mu Zhang, Niko Moses, Cong-Li Hu, Lisa Polin, Wei Chen, Hyejeong Jang, Joshua Heyza, Agnes Malysa, Joseph A Caruso and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 71 citations in OpenAlex.

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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

18 authors at 5 institutions in 2 countries.

Chen Hu *Department of Oncology, Karmanos Cancer Institute, Wayne State University, 4100 John R. St., Detroit, MI, 48201, USA.
Mu Zhang *Department of Oncology, Karmanos Cancer Institute, Wayne State University, 4100 John R. St., Detroit, MI, 48201, USA.
Niko MosesCancer Biology Graduate Program, Karmanos Cancer Institute, 4100 John R. St., Detroit, MI, 48201, USA.
Cong-Li HuInstitute of Translational Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, 201620, Shanghai, China.
Lisa PolinDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, 4100 John R. St., Detroit, MI, 48201, USA.
Wei ChenDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, 4100 John R. St., Detroit, MI, 48201, USA.
Hyejeong JangDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, 4100 John R. St., Detroit, MI, 48201, USA.
Joshua HeyzaCancer Biology Graduate Program, Karmanos Cancer Institute, 4100 John R. St., Detroit, MI, 48201, USA.
Agnes MalysaCancer Biology Graduate Program, Karmanos Cancer Institute, 4100 John R. St., Detroit, MI, 48201, USA.
Joseph A CarusoProteomics Facility Core, Institute of Environmental Health Sciences, Wayne State University, Scott Hall of Medical Sciences, 540 East Canfield, Room 2105, Detroit, MI, 48201, USA.ORCID http://orcid.org/0000-0003-2900-3996
Shengyan XiangDepartment of Pathology and Cell Biology, Morsani College of Medicine, University of South Florida, 12901 Bruce B. Downs Blvd., Tampa, FL, 33612, USA.
Steve PatrickDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, 4100 John R. St., Detroit, MI, 48201, USA.ORCID http://orcid.org/0000-0003-3325-6750
Paul StemmerProteomics Facility Core, Institute of Environmental Health Sciences, Wayne State University, Scott Hall of Medical Sciences, 540 East Canfield, Room 2105, Detroit, MI, 48201, USA.
Zhenkun LouDepartment of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.ORCID http://orcid.org/0000-0003-1938-3091
Wenlong BaiDepartment of Pathology and Cell Biology, Morsani College of Medicine, University of South Florida, 12901 Bruce B. Downs Blvd., Tampa, FL, 33612, USA.
Chuangui WangInstitute of Translational Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, 201620, Shanghai, China.
Gerold BeplerDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, 4100 John R. St., Detroit, MI, 48201, USA. beplerg@karmanos.org.
Xiaohong Mary ZhangDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, 4100 John R. St., Detroit, MI, 48201, USA. zhangx@karmanos.org.
Wayne State University · USShanghai Jiao Tong University · CNThe Barbara Ann Karmanos Cancer Institute · USUniversity of South Florida · USMayo Clinic in Arizona · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
Pilot Project ProgramP30ES020957 · NIEHS · WAYNE STATE UNIVERSITY · PI RUNGE-MORRIS, MELISSA A · 2014 to 2021
$10.1M
TRAINING PROGRAM IN THE BIOLOGY OF CANCERT32CA009531 · NCI · WAYNE STATE UNIVERSITY · PI Larry H Matherly · 1985 to 2026
$5.3M
Novel role of APOBEC3 enzymes as key mediators of cisplatin sensitivity through aberrant processing of interstrand crosslinksR01CA229535 · NCI · WAYNE STATE UNIVERSITY · PI PATRICK, STEVE M · 2019 to 2024
$2.0M
ROLE OF HDAC6 IN PLATINUM RESISTANCE OF NON-SMALL CELL LUNG CANCERR01CA164147 · NCI · WAYNE STATE UNIVERSITY · PI ZHANG, XIAOHONG MARY · 2012 to 2016
$1.6M
Orbitrap Velos with ETD for Wayne State ProteomicsS10OD010700 · OD · WAYNE STATE UNIVERSITY · PI STEMMER, PAUL M · 2012 to 2012
$575k
NCI NIH HHS P30 CA022453NCI NIH HHS R01 CA164147NCI NIH HHS R01 CA229535NCI NIH HHS T32 CA009531NIEHS NIH HHS P30 ES020957NIH HHS S10 OD010700
6 · The paper itself

Abstract

Ubiquitin-specific peptidase 10 (USP10) stabilizes both tumor suppressors and oncogenes in a context-dependent manner. However, the nature of USP10's role in non-small cell lung cancer (NSCLC) remains unclear. By analyzing The Cancer Genome Atlas (TCGA) database, we have shown that high levels of USP10 are associated with poor overall survival in NSCLC with mutant p53, but not with wild-type p53. Consistently, genetic depletion or pharmacological inhibition of USP10 dramatically reduces the growth of lung cancer xenografts lacking wild-type p53 and sensitizes them to cisplatin. Mechanistically, USP10 interacts with, deubiquitinates, and stabilizes oncogenic protein histone deacetylase 6 (HDAC6). Furthermore, reintroducing either USP10 or HDAC6 into a USP10-knockdown NSCLC H1299 cell line with null-p53 renders cisplatin resistance. This result suggests the existence of a "USP10-HDAC6-cisplatin resistance" axis. Clinically, we have found a positive correlation between USP10 and HDAC6 expression in a cohort of NSCLC patient samples. Moreover, we have shown that high levels of USP10 mRNA correlate with poor overall survival in a cohort of advanced NSCLC patients who received platinum-based chemotherapy. Overall, our studies suggest that USP10 could be a potential biomarker for predicting patient response to platinum, and that targeting USP10 could sensitize lung cancer patients lacking wild-type p53 to platinum-based therapy.

Indexed as

Drug Resistance, NeoplasmAnimalsCarcinoma, Non-Small-Cell LungCell Line, TumorCisplatinFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHistone Deacetylase 6HumansLung NeoplasmsMice, SCIDMutationOvarian NeoplasmsPlatinumProtein BindingCisplatinHistone Deacetylase 6PlatinumTumor Suppressor Protein p53Ubiquitin ThiolesteraseUSP10 protein, human

Identifiers

PMID32382008
PMCPMC7206099
OpenAlexW3022337093

What OpenQuestion holds

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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.