Evidence map›Paper›PMID 27598218›Full record

ArticleBiomolecules2016

An Epigenomic Approach to Improving Response to Neoadjuvant Cisplatin Chemotherapy in Bladder Cancer.

Evanguelos Xylinas, Melanie R Hassler, Dazhong Zhuang, Martin Krzywinski, Zeynep Erdem, Brian D Robinson, Olivier Elemento, Thomas Clozel, Shahrokh F Shariat

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
4.7field-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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. RASSF1A and its epigenetic dysregulation in genitourinary cancer: a current update.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Role of Epigenetics for the Efficacy of Cisplatin.International journal of molecular sciences · 2024
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. HighThe Journal of international medical research · 2022
    Article
  14. Response of the Urothelial Carcinoma Cell Lines to Cisplatin.International journal of molecular sciences · 2022
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

9 authors at 6 institutions in 4 countries.

Evanguelos XylinasDepartment of Urology, Weill Cornell Medical College, New York-Presbyterian Hospital, New York, NY 10065, USA. evanguelosxylinas@hotmail.com.
Melanie R HasslerDepartment of Urology, Medical University of Vienna, Vienna 1090, Austria. melanie.hassler@meduniwien.ac.at.
Dazhong ZhuangDepartment of Urology, Weill Cornell Medical College, New York-Presbyterian Hospital, New York, NY 10065, USA. dz100005@gmail.com.
Martin KrzywinskiCanada's Michael Smith Genome Sciences Center, Cancer Research Center, Vancouver, BC V5Z4S6, Canada. martink@bcgsc.ca.
Zeynep ErdemInstitute of Cancer Research, Department of Medicine 1, Medical University of Vienna, Vienna 1090, Austria. zeynep.erdem@meduniwien.ac.at.
Brian D RobinsonDepartment of Pathology, Weill Cornell Medical College, New York-Presbyterian Hospital, New York, NY 10065, USA. brr2006@med.cornell.edu.
Olivier ElementoDivision of Physiology and Biophysics, Weill Cornell Medical College, New York-Presbyterian Hospital, New York, NY 10065, USA. ole2001@med.cornell.edu.
Thomas ClozelDivision of Medical Oncology, Weill Cornell Medical College, New York-Presbyterian Hospital, New York, NY 10065, USA. thomas.clozel@gmail.com.
Shahrokh F ShariatDepartment of Urology, Weill Cornell Medical College, New York-Presbyterian Hospital, New York, NY 10065, USA. shahrokh.shariat@meduniwien.ac.at.
Presbyterian Hospital · USMedical University of Vienna · ATCanada's Michael Smith Genome Sciences Centre · CACornell University · USInserm · FRNewYork–Presbyterian Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bladder cancer is among the five most common cancers diagnosed in the Western world and causes significant mortality and morbidity rates in affected patients. Therapeutic options to treat the disease in advanced muscle-invasive bladder cancer (MIBC) include cystectomy and chemotherapy. Neoadjuvant cisplatin-based combination chemotherapy is effective in MIBC; however, it has not been widely adopted by the community. One reason is that many patients do not respond to neoadjuvant chemotherapy, and no biomarker currently exists to identify these patients. It is also not clear whether a strategy to sensitize chemoresistant patients may exist. We sought to identify cisplatin-resistance patterns in preclinical models of bladder cancer, and test whether treatment with the epigenetic modifier decitabine is able to sensitize cisplatin-resistant bladder cancer cell lines. Using a screening approach in cisplatin-resistant bladder cancer cell lines, we identified dysregulated genes by RNA sequencing (RNAseq) and DNA methylation assays. DNA methylation analysis of tumors from 18 patients receiving cisplatin-based chemotherapy was used to confirm in vitro results. Cisplatin-resistant bladder cancer cells were treated with decitabine to investigate epigenetic sensitization of resistant cell lines. Our results show that HOXA9 promoter methylation status is associated with response to cisplatin-based chemotherapy in bladder cancer cell lines and in metastatic bladder cancer. Bladder cancer cells resistant to cisplatin chemotherapy can be sensitized to cisplatin by the DNA methylation inhibitor decitabine. Our data suggest that HOXA9 promoter methylation could serve as potential predictive biomarker and decitabine might sensitize resistant tumors in patients receiving cisplatin-based chemotherapy.

Indexed as

Antineoplastic AgentsAzacitidineBiomarkers, TumorCell Line, TumorCisplatinDecitabineDoxorubicinDrug Resistance, NeoplasmEpigenomicsEtoposideHomeodomain ProteinsHumansHydroxamic AcidsMethylationNeoadjuvant TherapyPromoter Regions, GeneticAntineoplastic AgentsAzacitidineBiomarkers, TumorCisplatinDecitabineDoxorubicinEtoposidehomeobox protein HOXA9Homeodomain ProteinsHydroxamic AcidsVinblastineVorinostatdecitabinedrug resistanceHOXA9neoadjuvant therapyurinary bladder neoplasms

Identifiers

PMID27598218
PMCPMC5039423
OpenAlexW2515715601

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.