Evidence map›Paper›PMID 31600961›Full record

ArticleInternational journal of molecular sciences2019

Methionine Adenosyltransferase 1a (MAT1A) Enhances Cell Survival During Chemotherapy Treatment and is Associated with Drug Resistance in Bladder Cancer PDX Mice.

Kelly A Martin, Nicholas R Hum, Aimy Sebastian, Wei He, Salma Siddiqui, Paramita M Ghosh, Chong-Xian Pan, Ralph de Vere White, Gabriela G Loots

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Preclinical Models for Bladder Cancer Research.Hematology/oncology clinics of North America · 2021
    Review
  6. 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 2 institutions in 1 country.

Kelly A MartinLawrence Livermore National Laboratory, Physical and Life Sciences Directorate, Livermore, CA 94550, USA. martin249@llnl.gov.
Nicholas R HumLawrence Livermore National Laboratory, Physical and Life Sciences Directorate, Livermore, CA 94550, USA. hum3@llnl.gov.ORCID 0000-0003-1605-3193
Aimy SebastianLawrence Livermore National Laboratory, Physical and Life Sciences Directorate, Livermore, CA 94550, USA. sebastian4@llnl.gov.ORCID 0000-0002-7822-7040
Wei HeLawrence Livermore National Laboratory, Physical and Life Sciences Directorate, Livermore, CA 94550, USA. he4@llnl.gov.ORCID 0000-0003-2795-0324
Salma SiddiquiUC Davis Comprehensive Cancer Center, Sacramento, CA 95817, USA. SALMA.SIDDIQUI@va.gov.
Paramita M GhoshUC Davis Comprehensive Cancer Center, Sacramento, CA 95817, USA. paghosh@ucdavis.edu.ORCID 0000-0002-7304-2936
Chong-Xian PanUC Davis Comprehensive Cancer Center, Sacramento, CA 95817, USA. cxpan@ucdavis.edu.
Ralph de Vere WhiteUC Davis Comprehensive Cancer Center, Sacramento, CA 95817, USA. rwdeverewhite@ucdavis.edu.
Gabriela G LootsLawrence Livermore National Laboratory, Physical and Life Sciences Directorate, Livermore, CA 94550, USA. loots1@llnl.gov.ORCID 0000-0001-9546-5561
Lawrence Livermore National Laboratory · USUC Davis Comprehensive Cancer Center

Funding

University of California Minority Patient-Derived Xenograft (PDX) Development and Trial Center (UCaMP) to Reduce Cancer Health DisparitiesU54CA233306 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CARVAJAL CARMONA, LUIS GUILLERMO, CHEN, MOON SHAO-CHUANG · 2018 to 2022
$6.8M
Targeted-and timed-releasing nanotherapeutics against leukemia stem cellsR01CA176803 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PAN, CHONG-XIAN · 2015 to 2019
$1.8M
NCI NIH HHS R01 CA176803NCI NIH HHS U54 CA233306
6 · The paper itself

Abstract

Bladder cancer is among the top ten most common cancers, with about ~380,000 new cases and ~150,000 deaths per year worldwide. Tumor relapse following chemotherapy treatment has long been a significant challenge towards completely curing cancer. We have utilized a patient-derived bladder cancer xenograft (PDX) platform to characterize molecular mechanisms that contribute to relapse following drug treatment in advanced bladder cancer. Transcriptomic profiling of bladder cancer xenograft tumors by RNA-sequencing analysis, before and after relapse, following a 21-day cisplatin/gemcitabine drug treatment regimen identified methionine adenosyltransferase 1a (

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationCell SurvivalDisease Models, AnimalDrug Resistance, NeoplasmGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMethionine AdenosyltransferaseMiceTranscriptomeUrinary Bladder NeoplasmsXenograft Model Antitumor AssaysAntineoplastic AgentsMAT1A protein, humanMethionine Adenosyltransferasebladder cancerdrug resistancegemcitabinemethyltransferase

Identifiers

PMID31600961
PMCPMC6829260
OpenAlexW2979946309

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.