Evidence map›Paper›PMID 38990091›Full record

ArticleMolecular carcinogenesis2024

KDM1A/LSD1 inhibition enhances chemotherapy response in ovarian cancer.

Yihong Chen, Jessica D Johnson, Sridharan Jayamohan, Yi He, Prabhakar P Venkata, Diksha Jamwal, Salvador Alejo, Yi Zou, Zhao Lai, Suryavathi Viswanadhapalli and 3 more

Abstract read
In one paragraph

Article in Molecular carcinogenesis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Identification of epigenetic monotherapy candidates in taxane-resistant CRPC.Turkish journal of biology = Turk biyoloji dergisi · 2025
    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

13 authors.

Yihong ChenDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.
Jessica D JohnsonDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.
Sridharan JayamohanDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.
Yi HeDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.
Prabhakar P VenkataDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.
Diksha JamwalDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.
Salvador AlejoDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.ORCID 0000-0002-1390-9892
Yi ZouGreehey Children's Cancer Research Institute, UT Health San Antonio, San Antonio, Texas, USA.
Zhao LaiGreehey Children's Cancer Research Institute, UT Health San Antonio, San Antonio, Texas, USA.
Suryavathi ViswanadhapalliDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.
Ratna K VadlamudiDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.ORCID 0000-0003-2849-4076
Edward KostDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.
Gangadhara R SareddyDepartment of Obstetrics and Gynecology, UT Health San Antonio, San Antonio, Texas, USA.

Funding

Cancer Biology Training ProgramT32CA148724 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Pei Wang, Feng-Chun Yang · 2011 to 2026
$3.3M
Novel targeted therapy for treating Ovarian CancerR01CA266970 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Bindu Santhamma, Ratna K Vadlamudi · 2022 to 2026
$3.3M
Enhancing endoplasmic reticulum stress in ovarian cancerR01CA262757 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JUNG-MO AHN, Ratna K Vadlamudi · 2022 to 2026
$2.6M
KDM1A inhibitors as novel therapeutics for glioblastomaR01NS106173 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SAREDDY, GANGADHARA R · 2019 to 2023
$1.6M
Advancing Cancer Research Through Next Generation Sequencing at Mays Cancer Center of UT Health San AntonioR50CA265339 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Zhao Lai · 2022 to 2026
$957k
Illumina NovaSeq 6000 Sequencing SystemS10OD030311 · OD · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LAI, ZHAO · 2021 to 2021
$600k
American Cancer Society Research Scholar Grant 132931-RSG-18-187-01-TBGElsa U. Pardee Foundation GrantNational Institutes of Health: NIH-1R01NS106173-01A1National Institutes of Health: NIH-R01CA262757National Institutes of Health: NIH-R01CA266970-01A1National Institutes of Health: NIH-T32CA148724National Institutes of Health: R50-CA26533NCI NIH HHS R01 CA262757NCI NIH HHS R01 CA266970NCI NIH HHS R50 CA265339NCI NIH HHS T32 CA148724NIH HHS S10 OD030311NINDS NIH HHS R01 NS106173
6 · The paper itself

Abstract

Ovarian cancer (OCa) is the deadliest of all gynecological cancers. The standard treatment for OCa is platinum-based chemotherapy, such as carboplatin or cisplatin in combination with paclitaxel. Most patients are initially responsive to these treatments; however, nearly 90% will develop recurrence and inevitably succumb to chemotherapy-resistant disease. Recent studies have revealed that the epigenetic modifier lysine-specific histone demethylase 1A (KDM1A/LSD1) is highly overexpressed in OCa. However, the role of KDM1A in chemoresistance and whether its inhibition enhances chemotherapy response in OCa remains uncertain. Analysis of TCGA datasets revealed that KDM1A expression is high in patients who poorly respond to chemotherapy. Western blot analysis show that treatment with chemotherapy drugs cisplatin, carboplatin, and paclitaxel increased KDM1A expression in OCa cells. KDM1A knockdown (KD) or treatment with KDM1A inhibitors NCD38 and SP2509 sensitized established and patient-derived OCa cells to chemotherapy drugs in reducing cell viability and clonogenic survival and inducing apoptosis. Moreover, knockdown of KDM1A sensitized carboplatin-resistant A2780-CP70 cells to carboplatin treatment and paclitaxel-resistant SKOV3-TR cells to paclitaxel. RNA-seq analysis revealed that a combination of KDM1A-KD and cisplatin treatment resulted in the downregulation of genes related to epithelial-mesenchymal transition (EMT). Interestingly, cisplatin treatment increased a subset of NF-κB pathway genes, and KDM1A-KD or KDM1A inhibition reversed this effect. Importantly, KDM1A-KD, in combination with cisplatin, significantly reduced tumor growth compared to a single treatment in an orthotopic intrabursal OCa xenograft model. Collectively, these findings suggest that combination of KDM1A inhibitors with chemotherapy could be a promising therapeutic approach for the treatment of OCa.

Indexed as

CarboplatinCisplatinDrug Resistance, NeoplasmHistone DemethylasesOvarian NeoplasmsPaclitaxelXenograft Model Antitumor AssaysAnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsApoptosisCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansAntineoplastic AgentsCarboplatinCisplatinHistone DemethylasesHydrazinesKDM1A protein, humanPaclitaxelSP2509SulfonamideschemotherapyKDM1ALSD1ovarian cancer

Identifiers

PMID38990091
PMCPMC11421967

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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.