Evidence map›Paper›PMID 40698144›Full record

ReviewActa pharmaceutica Sinica. B2025

Artificial intelligence and anti-cancer drugs' response.

Xinrui Long, Kai Sun, Sicen Lai, Yuancheng Liu, Juan Su, Wangqing Chen, Ruhan Liu, Xiaoyu He, Shuang Zhao, Kai Huang

Abstract readReview
In one paragraph

Review in Acta pharmaceutica Sinica. B, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Acta pharmaceutica Sinica. B · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Drug response in the era of precision medicine: A methodological review.Computational and structural biotechnology journal · 2025
    Review
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.

Xinrui LongDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha 410028, China.
Kai SunDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha 410028, China.
Sicen LaiDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha 410028, China.
Yuancheng LiuDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha 410028, China.
Juan SuDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha 410028, China.
Wangqing ChenDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha 410028, China.
Ruhan LiuDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha 410028, China.
Xiaoyu HeDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha 410028, China.
Shuang ZhaoDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha 410028, China.
Kai HuangDepartment of Dermatology, Xiangya Hospital, Central South University, Changsha 410028, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug resistance is one of the key factors affecting the effectiveness of cancer treatment methods, including chemotherapy, radiotherapy, and immunotherapy. Its occurrence is related to factors such as mRNA expression and methylation within cancer cells. If drug resistance in patients can be accurately identified early, doctors can devise more effective treatment plans, which is of great significance for improving patients' survival rates and quality of life. Cancer drug resistance prediction based on artificial intelligence (AI) technology has emerged as a current research hotspot, demonstrating promising application prospects in guiding clinical individualized and precise medication for cancer patients. This review aims to comprehensively summarize the research progress in utilizing AI algorithms to analyze multi-omics data including genomics, transcriptomics, epigenomics, proteomics, metabolomics, radiomics, and histopathology, for predicting cancer drug resistance. It provides a detailed exposition of the processes involved in data processing and model construction, examines the current challenges faced in this field and future development directions, with the aim of better advancing the progress of precision medicine.

Indexed as

Anti-cancer drugsArtificial intelligenceDrug resistanceMulti-omicsPrecision medication

Identifiers

PMID40698144
PMCPMC12278413

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.