Evidence map›Paper›PMID 35817212›Full record

ReviewAdvanced drug delivery reviews2022

HuR as a molecular target for cancer therapeutics and immune-related disorders.

Mrinmoyee Majumder, Paramita Chakraborty, Sarumathi Mohan, Shikhar Mehrotra, Viswanathan Palanisamy

Open access · greenAbstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
10.2field-weighted citation impact, top 1% 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

74 citing papers in PubMed, 116 citations in OpenAlex.

  1. Article
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  10. Potential role ofBiochemistry and biophysics reports · 2026
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14 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Mrinmoyee MajumderDepartment of Biochemistry and Molecular Biology, Charleston, SC 29425, USA.
Paramita ChakrabortyDepartment of Surgery, College of Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.
Sarumathi MohanDepartment of Biochemistry and Molecular Biology, Charleston, SC 29425, USA.
Shikhar MehrotraDepartment of Surgery, College of Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.
Viswanathan PalanisamyDepartment of Biochemistry and Molecular Biology, Charleston, SC 29425, USA. Electronic address: visu@musc.edu.
University of Charleston · USMedical University of South Carolina · US

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
Anti-oxidant and Metabolic Phenotype in Regulating Tumor Specific T cell Memory ResponseR01CA236379 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MEHROTRA, SHIKHAR · 2020 to 2024
$2.5M
Intersections of RNA-binding proteins and T-cells in oral epithelial plasticityR01DE030013 · NIDCR · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI MEHROTRA, SHIKHAR, PALANISAMY, VISWANATHAN · 2020 to 2024
$2.3M
Targeting of RNA-binding protein FXR1 in HNSCCR21DE032461 · NIDCR · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI PALANISAMY, VISWANATHAN · 2023 to 2023
$419k
NCATS NIH HHS UL1 TR001450NCI NIH HHS R01 CA236379NIDCR NIH HHS R01 DE030013NIDCR NIH HHS R21 DE032461
6 · The paper itself

Abstract

The control of eukaryotic gene expression occurs at multiple levels, from transcription to messenger RNA processing, transport, localization, turnover, and translation. RNA-binding proteins control gene expression and are involved in different stages of mRNA processing, including splicing, maturation, turnover, and translation. A ubiquitously expressed RBP Human antigen R is engaged in the RNA processes mentioned above but, most importantly, controls mRNA stability and turnover. Dysregulation of HuR is linked to many diseases, including cancer and other immune-related disorders. HuR targets mRNAs containing AU-rich elements at their 3'untranslated region, which encodes proteins involved in cell growth, proliferation, tumor formation, angiogenesis, immune evasion, inflammation, invasion, and metastasis. HuR overexpression has been reported in many tumor types, which led to a poor prognosis for patients. Hence, HuR is considered an appealing drug target for cancer treatment. Therefore, multiple attempts have been made to identify small molecule inhibitors for blocking HuR functions. This article reviews the current prospects of drugs that target HuR in numerous cancer types, their mode of action, and off-target effects. Furthermore, we will summarize drugs that interfered with HuR-RNA interactions and established themselves as novel therapeutics. We will also highlight the significance of HuR overexpression in multiple cancers and discuss its role in immune functions. This review provides evidence of a new era of HuR-targeted small molecules that can be used for cancer therapeutics either as a monotherapy or in combination with other cancer treatment modalities.

Indexed as

ELAV-Like Protein 1NeoplasmsHumansNeovascularization, PathologicRNA-Binding ProteinsRNA, MessengerELAVL1 protein, humanELAV-Like Protein 1RNA-Binding ProteinsRNA, MessengerCancer growth and progression and small-molecule inhibitorsmRNA translationmRNA turnoverPosttranscriptional gene regulationRNA-binding proteins

Identifiers

PMID35817212
PMCPMC10276344
OpenAlexW4284974998

What OpenQuestion holds

Textmetadata
LicenceTDM
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.