Evidence map›Paper›PMID 30323891›Full record

ArticleOncotarget2018

TRPV2 is a novel biomarker and therapeutic target in triple negative breast cancer.

Mohamad Elbaz, Dinesh Ahirwar, Zhang Xiaoli, Xinyu Zhou, Maryam Lustberg, Mohd W Nasser, Konstantin Shilo, Ramesh K Ganju

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 12% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

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  17. Blockade of TRPV channels by intracellular spermine.The Journal of general physiology · 2023
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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

8 authors at 3 institutions in 2 countries.

Mohamad ElbazDepartment of Pathology, Wexner Medical Center, Ohio State University (OSU), Columbus, OH, USA.
Dinesh AhirwarDepartment of Pathology, Wexner Medical Center, Ohio State University (OSU), Columbus, OH, USA.
Zhang XiaoliCenter for Biostatistics, Ohio State University (OSU), Columbus, OH, USA.
Xinyu ZhouDepartment of surgery, Davis Heart and Lung Research Institute, Ohio State University, Columbus, OH, USA.
Maryam LustbergDepartment of Internal Medicine, Ohio State University (OSU), Columbus, OH, USA.
Mohd W NasserDepartment of Pathology, Wexner Medical Center, Ohio State University (OSU), Columbus, OH, USA.
Konstantin ShiloDepartment of Pathology, Wexner Medical Center, Ohio State University (OSU), Columbus, OH, USA.
Ramesh K GanjuDepartment of Pathology, Wexner Medical Center, Ohio State University (OSU), Columbus, OH, USA.
The Ohio State University Wexner Medical Center · USThe Ohio State University · USLung Institute · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Role of Slit in CXCR4-Mediated Breast Cancer MetastasisR01CA109527 · NCI · OHIO STATE UNIVERSITY · PI GANJU, RAMESH K. · 2005 to 2019
$2.6M
Role of S100A7 in breast cancer progression and metastasisR01CA153490 · NCI · OHIO STATE UNIVERSITY · PI GANJU, RAMESH K. · 2011 to 2014
$1.2M
NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA109527NCI NIH HHS R01 CA153490
6 · The paper itself

Abstract

Transient receptor potential vanilloid type-2 (TRPV2) is an ion channel that is triggered by agonists like cannabidiol (CBD). Triple negative breast cancer (TNBC) is an aggressive disease with limited therapeutic options. Chemotherapy is still the first line for the treatment of TNBC patients; however, TNBC usually gains rapid resistance and unresponsiveness to chemotherapeutic drugs. In this study, we found that TRPV2 protein is highly up-regulated in TNBC tissues compared to normal breast tissues. We also observed that TNBC and estrogen receptor alpha negative (ERβ-) patients with higher TRPV2 expression have significantly higher recurrence free survival compared to patients with lower TRPV2 expression especially those who were treated with chemotherapy. In addition, we showed that TRPV2 overexpression or activation by CBD significantly increased doxorubicin (DOX) uptake and apoptosis in TNBC cells. The induction of DOX uptake was abrogated by TRPV2 blocking or downregulation.

Indexed as

chemotherapydoxorubicinTNBCTRPV2uptake

Identifiers

PMID30323891
PMCPMC6173360
OpenAlexW2401330861

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.