Evidence map›Paper›PMID 40681956›Full record

ArticleFunctional & integrative genomics2025

ALKBH5-mediated NPC2 mRNA m

Peng Wan, Yuan Ren, Hong-Tao Li

Abstract read
In one paragraph

Article in Functional & integrative genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

3 authors.

Peng Wan *Department of Oncology, The First Affiliated Hospital of Yangtze University, Jing Zhou, Hubei, 434000, China.
Yuan Ren *Department of Oncology, The First Affiliated Hospital of Yangtze University, Jing Zhou, Hubei, 434000, China.
Hong-Tao LiDepartment of Oncology, The First Affiliated Hospital of Yangtze University, Jing Zhou, Hubei, 434000, China. hbssLht@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is the third most common cancer globally and a leading cause of cancer-related death. Oxaliplatin, a key platinum-based chemotherapy, significantly improves outcomes in CRC patients. Nevertheless, oxaliplatin resistance often emerges, leading to worse prognosis. Exploring new biomarkers and mechanisms of resistance is crucial for overcoming oxaliplatin resistance and enhancing therapeutic efficacy. Through bioinformatics analysis, high NPC2 expression was found to be associated with oxaliplatin resistance and poor prognosis in CRC patients. Moreover, NPC2 was highly expressed in CRC tissues, especially in metastatic CRC tissues. Additionally, the expression of N6-methyladenosine (m

Indexed as

AlkB Homolog 5, RNA DemethylaseColorectal NeoplasmsDrug Resistance, NeoplasmOxaliplatinAdenosineAnimalsCell Line, TumorDemethylationFemaleGene Expression Regulation, NeoplasticHumansMaleMiceMice, NudeRNA-Binding ProteinsRNA, MessengerAdenosineALKBH5 protein, humanAlkB Homolog 5, RNA DemethylaseN-methyladenosineOxaliplatinRNA-Binding ProteinsRNA, MessengerYTHDF2 protein, humanALKBH5Colorectal cancerm6ANPC2Oxaliplatin resistance

Identifiers

PMID40681956
PMCPMC12274260

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.