Evidence map›Paper›PMID 36254250›Full record

ReviewMedComm2022

Small molecule inhibitors targeting the cancers.

Gui-Hong Liu, Tao Chen, Xin Zhang, Xue-Lei Ma, Hua-Shan Shi

Abstract readReview
In one paragraph

Review in MedComm, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed, 1 pooled it
–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

102 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Thieno[3,2-International journal of molecular sciences · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Circulating Tumor Cells: Emerging Frontiers in Cancer Technology.Expert reviews in molecular medicine · 2026
    Review
  17. Review
  18. Article
  19. Asian journal of pharmaceutical sciences · 2026
    Article
  20. Article

42 more citing papers are in PubMed but not listed here.

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.

Gui-Hong LiuDepartment of Biotherapy State Key Laboratory of Biotherapy Cancer Center, West China Hospital Sichuan University Chengdu China.ORCID https://orcid.org/0000-0002-1140-5359
Tao ChenDepartment of Cardiology The First Affiliated Hospital of China Medical University Shenyang Liaoning China.
Xin ZhangDepartment of Biotherapy State Key Laboratory of Biotherapy Cancer Center, West China Hospital Sichuan University Chengdu China.
Xue-Lei MaDepartment of Biotherapy State Key Laboratory of Biotherapy Cancer Center, West China Hospital Sichuan University Chengdu China.ORCID https://orcid.org/0000-0002-9148-5001
Hua-Shan ShiDepartment of Biotherapy State Key Laboratory of Biotherapy Cancer Center, West China Hospital Sichuan University Chengdu China.ORCID https://orcid.org/0000-0002-9958-9892

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Compared with traditional therapies, targeted therapy has merits in selectivity, efficacy, and tolerability. Small molecule inhibitors are one of the primary targeted therapies for cancer. Due to their advantages in a wide range of targets, convenient medication, and the ability to penetrate into the central nervous system, many efforts have been devoted to developing more small molecule inhibitors. To date, 88 small molecule inhibitors have been approved by the United States Food and Drug Administration to treat cancers. Despite remarkable progress, small molecule inhibitors in cancer treatment still face many obstacles, such as low response rate, short duration of response, toxicity, biomarkers, and resistance. To better promote the development of small molecule inhibitors targeting cancers, we comprehensively reviewed small molecule inhibitors involved in all the approved agents and pivotal drug candidates in clinical trials arranged by the signaling pathways and the classification of small molecule inhibitors. We discussed lessons learned from the development of these agents, the proper strategies to overcome resistance arising from different mechanisms, and combination therapies concerned with small molecule inhibitors. Through our review, we hoped to provide insights and perspectives for the research and development of small molecule inhibitors in cancer treatment.

Indexed as

combination therapymultikinase molecule inhibitorsresistancesmall molecule inhibitorssmall molecule kinase inhibitors

Identifiers

PMID36254250
PMCPMC9560750

What OpenQuestion holds

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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.