Evidence map›Paper›PMID 32498332›Full record

ArticleCancers2020

Rlip Depletion Suppresses Growth of Breast Cancer.

Chhanda Bose, Sushma Yadav, Sharad S Singhal, Jyotsana Singhal, Ashly Hindle, Jihyun Lee, Naga K S Cheedella, Shabnam Rehman, Rakhshanda Layeequr Rahman, Catherine Jones and 5 more

Abstract read
In one paragraph

Article in Cancers, 2020. 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. Rlip76: An Unexplored Player in Neurodegeneration and Alzheimer's Disease?International journal of molecular sciences · 2022
    Review
  3. Article
  4. Article
  5. Article
  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

15 authors.

Chhanda BoseDepartment of Internal Medicine, Division of Hematology & Oncology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Sushma YadavDepartment of Translational Research and Cellular Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA 910102, USA.
Sharad S SinghalDepartment of Medical Oncology and Therapeutic Research, City of Hope Comprehensive Cancer Center, Duarte, CA 910102, USA.
Jyotsana SinghalDepartment of Medical Oncology and Therapeutic Research, City of Hope Comprehensive Cancer Center, Duarte, CA 910102, USA.
Ashly HindleDepartment of Internal Medicine, Division of Hematology & Oncology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Jihyun LeeDepartment of Internal Medicine, Division of Hematology & Oncology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Naga K S CheedellaDepartment of Internal Medicine, Division of Hematology & Oncology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Shabnam RehmanDepartment of Internal Medicine, Division of Hematology & Oncology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Rakhshanda Layeequr RahmanUniversity Medical Center Health System, UMC Cancer Center, Lubbock, TX 79415, USA.
Catherine JonesDepartment of Internal Medicine, Division of Hematology & Oncology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Meenakshi DardenMcGovern Medical School of the University of Texas Health Sciences Center, Houston, TX 77030, USA.
Philip T PaladeDepartment of Pharmacology and Toxicology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
David BerzBeverly Hills Cancer Center, Los Angeles, CA 90211, USA.
Sharda P SinghDepartment of Internal Medicine, Division of Hematology & Oncology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.ORCID 0000-0003-4361-4558
Sanjay AwasthiDepartment of Internal Medicine, Division of Hematology & Oncology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.ORCID 0000-0002-5214-5717

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RLIP76 (RAL-binding protein-1, Rlip) is a stress-protective mercapturic-acid-pathway transporter protein that also plays a key role in regulating clathrin-dependent endocytosis as a Ral effector. Targeted inhibition or depletion of Rlip causes regression of xenografts of many cancers and is capable of abrogating tumor formation in p53-null mice. This is associated with the reversion of the abnormal methylomic profile of p53-null mice to wild-type. In a query of The Cancer Genome Atlas (TCGA) databases, we found that Rlip expression was associated with poor survival and with significant differences in the frequencies of

Indexed as

apoptosisbreast cancerendocytosisRalBP1Rlip76

Identifiers

PMID32498332
PMCPMC7352702

What OpenQuestion holds

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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.