Evidence map›Paper›PMID 35251993›Full record

ArticleFrontiers in oncology2022

Pamela S VanderVere-Carozza, Navnath S Gavande, Shadia I Jalal, Karen E Pollok, Elmira Ekinci, Joshua Heyza, Steve M Patrick, Andi Masters, John J Turchi, Katherine S Pawelczak

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Re-establishment of TAD boundary organization during DNA replication.bioRxiv : the preprint server for biology · 2026
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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

10 authors at 5 institutions in 1 country.

Pamela S VanderVere-CarozzaDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States.
Navnath S GavandeDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States.
Shadia I JalalDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States.
Karen E PollokHerman B. Wells Center for Pediatric Research, Departments of Pediatrics, Pharmacology and Toxicology, Medical and Molecular Genetics Indiana University Simon Comprehensive Cancer Center, Indianapolis, IN, United States.
Elmira EkinciDepartment of Oncology, Wayne State University School of Medicine and Barbara Ann Karmanos Cancer Institute, Detroit, MI, United States.
Joshua HeyzaDepartment of Oncology, Wayne State University School of Medicine and Barbara Ann Karmanos Cancer Institute, Detroit, MI, United States.
Steve M PatrickDepartment of Oncology, Wayne State University School of Medicine and Barbara Ann Karmanos Cancer Institute, Detroit, MI, United States.
Andi MastersIndiana University Cancer Center, Indiana University School of Medicine, Indianapolis, IN, United States.
John J TurchiDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States.
Katherine S PawelczakNERx BioSciences, Indianapolis, IN, United States.
Indiana University – Purdue University Indianapolis · USIndiana University School of MedicineThe Barbara Ann Karmanos Cancer Institute · USNĒRx BioSciences (United States) · USWayne State University · US

Funding

Novel DNA damage response therapeutics targeting replication protein AR01CA257430 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI TURCHI, JOHN J. · 2021 to 2025
$2.4M
Novel role of APOBEC3 enzymes as key mediators of cisplatin sensitivity through aberrant processing of interstrand crosslinksR01CA229535 · NCI · WAYNE STATE UNIVERSITY · PI PATRICK, STEVE M · 2019 to 2024
$2.0M
NCI NIH HHS R01 CA229535NCI NIH HHS R01 CA257430
6 · The paper itself

Abstract

Replication protein A (RPA) plays essential roles in DNA replication, repair, recombination, and the DNA damage response (DDR). Retrospective analysis of lung cancer patient data demonstrates high RPA expression as a negative prognostic biomarker for overall survival in smoking-related lung cancers. Similarly, relative expression of RPA is a predictive marker for response to chemotherapy. These observations are consistent with the increase in RPA expression serving as an adaptive mechanism that allows tolerance of the genotoxic stress resulting from carcinogen exposure. We have developed second-generation RPA inhibitors (RPAis) that block the RPA-DNA interaction and optimized formulation for

Indexed as

DNA damage responseDNA repair and cancerDNA repair inhibitorsReplication Protein AReplication Stress Response

Identifiers

PMID35251993
PMCPMC8895377
OpenAlexW4213265657

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.