Evidence map›Paper›PMID 37359373›Full record

ArticleFrontiers in genetics2023

Destabilized 3'UTR elements therapeutically degrade ERBB2 mRNA in drug-resistant ERBB2+ cancer models.

Chidiebere U Awah, Yana Glemaud, Fayola Levine, Kiseok Yang, Afrin Ansary, Fu Dong, Leonard Ash, Junfei Zhang, Olorunseun O Ogunwobi

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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 3 institutions in 1 country.

Chidiebere U AwahDepartment of Biological Sciences, Hunter College of The City University of New York, New York City, NY, United States.
Yana GlemaudDepartment of Biological Sciences, Hunter College of The City University of New York, New York City, NY, United States.
Fayola LevineDepartment of Biological Sciences, Hunter College of The City University of New York, New York City, NY, United States.
Kiseok YangDepartment of Biological Sciences, Hunter College of The City University of New York, New York City, NY, United States.
Afrin AnsaryDepartment of Biological Sciences, Hunter College of The City University of New York, New York City, NY, United States.
Fu DongDepartment of Biological Sciences, Hunter College of The City University of New York, New York City, NY, United States.
Leonard AshDepartment of Biological Sciences, Hunter College of The City University of New York, New York City, NY, United States.
Junfei ZhangDepartment of Pathology and Cell Biology, Department of System Biology, Columbia University Medical Center, New York, NY, United States.
Olorunseun O OgunwobiDepartment of Biological Sciences, Hunter College of The City University of New York, New York City, NY, United States.
City University of New York · USHunter College · USColumbia University Irving Medical Center · US

Funding

TUFCCC/HC Regional Comprehensive Cancer Health PartnershipU54CA221704 · NCI · HUNTER COLLEGE · PI Ming-Chin Yeh · 2018 to 2026
$10.6M
NCI NIH HHS U54 CA221704
6 · The paper itself

Abstract

Breast, lung, and colorectal cancer resistance to molecular targeted therapy is a major challenge that unfavorably impacts clinical outcomes leading to hundreds of thousands of deaths annually. In ERBB2+ cancers regardless of the tissue of origin, many ERBB2+ cancers are resistant to ERBB2-targeted therapy. We discovered that ERBB2+ cancer cells are enriched with poly U sequences on their 3'UTR which are mRNA-stabilizing sequences. We developed a novel technology, in which we engineered these ERBB2 mRNA-stabilizing sequences to unstable forms that successfully overwrote and outcompeted the endogenous ERBB2 mRNA-encoded message and degraded ERBB2 transcripts which led to the loss of the protein across multiple cancer cell types both in the wildtype and drug-resistance settings

Indexed as

3'UTR elementscancercancer treatmentdrug resistanceERBB2 (HER2/neu)mRNA overwritingmRNA stabilizing

Identifiers

PMID37359373
PMCPMC10287955
OpenAlexW4380360831

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.