Evidence map›Paper›PMID 36945474›Full record

ArticlebioRxiv : the preprint server for biology2023

Identification of chemotherapy targets reveals a nucleus-to-mitochondria ROS sensing pathway.

Junbing Zhang, Claire M Simpson, Jacqueline Berner, Harrison B Chong, Jiafeng Fang, Zehra Ordulu Sahin, Tom Weiss-Sadan, Anthony P Possemato, Stefan Harry, Mariko Takahashi and 26 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

36 authors at 4 institutions in 1 country.

Junbing Zhang
Claire M Simpson
Jacqueline Berner
Harrison B Chong
Jiafeng Fang
Zehra Ordulu Sahin
Tom Weiss-Sadan
Anthony P Possemato
Stefan Harry
Mariko Takahashi
Tzu-Yi Yang
Marianne Richter
Himani Patel
Abby E Smith
Alexander D Carlin
Adriaan F Hubertus de Groot
Konstantin Wolf
Lei Shi
Ting-Yu Wei
Benedikt R Dürr
Nicholas J Chen
Tristan Vornbäumen
Nina O Wichmann
Venkatesh Pooladanda
Yuske Matoba
Shaan Kumar
Eugene Kim
Sara Bouberhan
Esther Olivia
Bo Rueda
Nabeel Bardeesy
Brian Liau
Michael Lawrence
Matt P Stokes
Sean A Beausoleil
Liron Bar-Peled
Massachusetts General Hospital · USHarvard University · USCell Signaling Technology (United States) · USUniversity of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple chemotherapies are proposed to cause cell death in part by increasing the steady-state levels of cellular reactive oxygen species (ROS). However, for most of these drugs exactly how the resultant ROS function and are sensed is poorly understood. In particular, it's unclear which proteins the ROS modify and their roles in chemotherapy sensitivity/resistance. To answer these questions, we examined 11 chemotherapies with an integrated proteogenomic approach identifying many unique targets for these drugs but also shared ones including ribosomal components, suggesting one mechanism by which chemotherapies regulate translation. We focus on CHK1 which we find is a nuclear H

Identifiers

PMID36945474
PMCPMC10028958
OpenAlexW4323980425

What OpenQuestion holds

Textmetadata
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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.