Evidence map›Paper›PMID 35625898›Full record

ArticleBiomedicines2022

Targeted Inhibition of O-Linked β-N-Acetylglucosamine Transferase as a Promising Therapeutic Strategy to Restore Chemosensitivity and Attenuate Aggressive Tumor Traits in Chemoresistant Urothelial Carcinoma of the Bladder.

Hye Won Lee, Mi Ju Kang, Young-Ju Kwon, Sama Abdi Nansa, Eui Hyun Jung, Sung Han Kim, Sang-Jin Lee, Kyung-Chae Jeong, Youngwook Kim, Heesun Cheong and 1 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. 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
0.6field-weighted citation impact, top 36% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
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  6. Review
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

11 authors at 1 institution in 1 country.

Hye Won LeeDepartment of Urology, Center for Urologic Cancer, National Cancer Center, Goyang 10408, Korea.
Mi Ju KangResearch Institute, National Cancer Center, Goyang 10408, Korea.
Young-Ju KwonResearch Institute, National Cancer Center, Goyang 10408, Korea.
Sama Abdi NansaDepartment of Cancer Biomedical Science, Graduate School of Cancer Science and Policy, National Cancer Center, Goyang 10408, Korea.ORCID 0000-0003-3410-0619
Eui Hyun JungDepartment of Urology, Center for Urologic Cancer, National Cancer Center, Goyang 10408, Korea.
Sung Han KimDepartment of Urology, Center for Urologic Cancer, National Cancer Center, Goyang 10408, Korea.
Sang-Jin LeeResearch Institute, National Cancer Center, Goyang 10408, Korea.
Kyung-Chae JeongResearch Institute, National Cancer Center, Goyang 10408, Korea.
Youngwook KimDepartment of Cancer Biomedical Science, Graduate School of Cancer Science and Policy, National Cancer Center, Goyang 10408, Korea.
Heesun CheongResearch Institute, National Cancer Center, Goyang 10408, Korea.ORCID 0000-0003-1946-107X
Ho Kyung SeoDepartment of Urology, Center for Urologic Cancer, National Cancer Center, Goyang 10408, Korea.
National Cancer Center · KR

Funding

National Cancer Center NCC-2210760National Research Foundation of Korea 2020R1A2B5B01002011
6 · The paper itself

Abstract

Acquisition of acquired chemoresistance during treatment cycles in urothelial carcinoma of the bladder (UCB) is the major cause of death through enhancing the risk of cancer progression and metastasis. Elevated glucose flux through the abnormal upregulation of O-linked β-N-acetylglucosamine (O-GlcNAc) transferase (OGT) controls key signaling and metabolic pathways regulating diverse cancer cell phenotypes. This study showed that OGT expression levels in two human UCB cell models with acquired resistance to gemcitabine and paclitaxel were significantly upregulated compared with those in parental cells. Reducing hyper-O-GlcNAcylation by OGT knockdown (KD) markedly facilitated chemosensitivity to the corresponding chemotherapeutics in both cells, and combination treatment with OGT-KD showed more severe growth defects in chemoresistant sublines. We subsequently verified the suppressive effects of OGT-KD monotherapy on cell migration/invasion in vitro and xenograft tumor growth in vivo in chemoresistant UCB cells. Transcriptome analysis of these cells revealed 97 upregulated genes, which were enriched in multiple oncogenic pathways. Our final choice of suspected OGT glycosylation substrate was VCAN, S1PR3, PDGFRB, and PRKCG, the knockdown of which induced cell growth defects. These findings demonstrate the vital role of dysregulated OGT activity and hyper-O-GlcNAcylation in modulating treatment failure and tumor aggression in chemoresistant UCB.

Indexed as

biomarkerschemoresistancegemcitabineO-linked N-acetylglucosaminylationO-linked β-N-acetylglucosamine transferasepaclitaxelurothelial carcinoma of bladder

Identifiers

PMID35625898
PMCPMC9138654
OpenAlexW4280643027

What OpenQuestion holds

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Read underepoch 390

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.