Evidence map›Paper›PMID 37389562›Full record

ArticleThe Journal of international medical research2023

Impact of cytotoxic chemotherapy on aldo-keto reductase family 1 member B10 expression.

Kathy Robinson, Zhe Cao, Kristin Delfino, Deliang Cao, Krishna Rao

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 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, top 74% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 countries.

Kathy RobinsonSimmons Cancer Institute, Southern Illinois University, Springfield, IL, USA.
Zhe CaoHunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Kristin DelfinoCenter for Clinical Research, Southern Illinois University, Springfield, IL, USA.
Deliang CaoHunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Krishna RaoDivision of Hematology/Oncology, Simmons Cancer Institute, Southern Illinois University, Springfield, IL, USA.ORCID 0000-0002-1788-264X
Southern Illinois University School of Medicine · USCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAldo-keto reductase family 1 member B10 (AKR1B10) is a protein that is produced and secreted by a significant number of breast cancers. However, a potential confounder to the use of AKR1B10 as a tumor marker is its elevation in patients given cytotoxic chemotherapy. We therefore conducted a prospective study to analyze AKR1B10 levels in patients with breast cancer receiving neoadjuvant cytotoxic chemotherapy.

methodsThe study enrolled 10 patients from November 2015 to July 2017. All patients had locally advanced, but non-metastatic, breast cancer, and they received neoadjuvant chemotherapy followed by surgery. Serum AKR1B10 levels and tumor imaging were assessed before, during, and after chemotherapy.

resultsNo increase in serum AKR1B10 levels was noted in patients receiving chemotherapy whose levels were elevated at diagnosis.

conclusionThe findings are complex, but the overall data suggest that AKR1B10 is suitable as a tumor marker in patients with elevated levels at the time of diagnosis.

Indexed as

Aldo-Keto Reductase Family 1 member B10Breast NeoplasmsBiological TransportBiomarkers, TumorFemaleHumansProspective StudiesAldo-Keto Reductase Family 1 member B10Biomarkers, TumorAldo-keto reductase family 1 member B10breast cancercytotoxic chemotherapyhormone receptorneoadjuvant therapysurgerytreatment responsetumor marker

Identifiers

PMID37389562
PMCPMC10328017
OpenAlexW4382631704

What OpenQuestion holds

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Registered trials

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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.