Evidence map›Paper›PMID 37020040›Full record

ArticleOncogene2023

ROS-mediated SRMS activation confers platinum resistance in ovarian cancer.

Yunhan Jiang, Lina Song, Yizhu Lin, Pawel Nowialis, Qiongmei Gao, Tao Li, Bin Li, Xiaobo Mao, Qianqian Song, Chengguo Xing and 3 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 22% 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, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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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

13 authors at 5 institutions in 1 country.

Yunhan JiangDepartment of Molecular Medicine, Long School of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA.ORCID 0000-0003-4941-1700
Lina SongDepartment of Molecular Medicine, Long School of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA.
Yizhu LinDepartment of Cell and Tissue Biology, School of Dentistry, University of California San Francisco, San Francisco, CA, 94143, USA.
Pawel NowialisDepartment of Molecular Medicine, Long School of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA.
Qiongmei GaoDepartment of Molecular Medicine, Long School of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA.
Tao LiDepartment of Anatomy and Cell Biology, College of Medicine, University of Florida, Gainesville, FL, 32610, USA.
Bin LiDepartment of Anatomy and Cell Biology, College of Medicine, University of Florida, Gainesville, FL, 32610, USA.
Xiaobo MaoInstitute for Cell Engineering, Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, 21205, USA.
Qianqian SongDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, NC, 27101, USA.ORCID 0000-0002-4455-5302
Chengguo XingDepartment of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, FL, 32610, USA.
Guangrong ZhengDepartment of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, FL, 32610, USA.ORCID 0000-0002-8106-6663
Shuang HuangDepartment of Anatomy and Cell Biology, College of Medicine, University of Florida, Gainesville, FL, 32610, USA.ORCID 0000-0002-9674-2249
Lingtao JinDepartment of Molecular Medicine, Long School of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA. jinl1@uthscsa.edu.ORCID 0009-0005-8106-3250
The University of Texas Health Science Center at San Antonio · USUniversity of Florida · USJohns Hopkins University · USUniversity of California, San Francisco · USWake Forest University · US

Funding

The role of NFIB-MAST1 signaling in mediating adaptive cisplatin resistance in SCLCR37CA249305 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lingtao Jin · 2020 to 2026
$2.9M
Novel protein kinase signaling associated with platinum resistance in ovarian cancerR01CA256482 · NCI · UNIVERSITY OF FLORIDA · PI HUANG, SHUANG, SONG, LINA · 2021 to 2025
$2.2M
The role of platinum-regulated lipid metabolism in tau-related dementiaR01CA269782 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lingtao Jin · 2022 to 2026
$2.2M
Impact of microRNA processing on EMT of ovarian cancer cellsR01CA222467 · NCI · UNIVERSITY OF FLORIDA · PI HUANG, SHUANG · 2018 to 2022
$1.7M
NCI NIH HHS R01 CA222467NCI NIH HHS R01 CA256482NCI NIH HHS R01 CA269782NCI NIH HHS R37 CA249305
6 · The paper itself

Abstract

Ovarian cancer is the leading cause of death among gynecological malignancies. Checkpoint blockade immunotherapy has so far only shown modest efficacy in ovarian cancer and platinum-based chemotherapy remains the front-line treatment. Development of platinum resistance is one of the most important factors contributing to ovarian cancer recurrence and mortality. Through kinome-wide synthetic lethal RNAi screening combined with unbiased datamining of cell line platinum response in CCLE and GDSC databases, here we report that Src-Related Kinase Lacking C-Terminal Regulatory Tyrosine And N-Terminal Myristylation Sites (SRMS), a non-receptor tyrosine kinase, is a novel negative regulator of MKK4-JNK signaling under platinum treatment and plays an important role in dictating platinum efficacy in ovarian cancer. Suppressing SRMS specifically sensitizes p53-deficient ovarian cancer cells to platinum in vitro and in vivo. Mechanistically, SRMS serves as a "sensor" for platinum-induced ROS. Platinum treatment-induced ROS activates SRMS, which inhibits MKK4 kinase activity by directly phosphorylating MKK4 at Y269 and Y307, and consequently attenuates MKK4-JNK activation. Suppressing SRMS leads to enhanced MKK4-JNK-mediated apoptosis by inhibiting MCL1 transcription, thereby boosting platinum efficacy. Importantly, through a "drug repurposing" strategy, we uncovered that PLX4720, a small molecular selective inhibitor of B-RafV

Indexed as

Ovarian NeoplasmsPlatinumCell Line, TumorDrug Resistance, NeoplasmFemaleHumansIndolesNeoplasm Recurrence, LocalReactive Oxygen Speciessrc-Family KinasesSulfonamidesIndolesPlatinumPLX 4720Reactive Oxygen Speciessrc-Family KinasesSulfonamides

Identifiers

PMID37020040
PMCPMC10231978
OpenAlexW4362636594

What Socratic holds

Textmetadata
LicenceTDM
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.