Evidence map›Paper›PMID 40944871›Full record

ReviewCancer chemotherapy and pharmacology2025

Anlotinib in cancer therapy: mechanisms of action, clinical applications, and future perspectives.

Jianhua Ding, Chai Hong Yeong, Lei Wang, Chunyan Shi, Long Li, Lijun Song, Wenxiu Ma, Peng Li

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cancer chemotherapy and pharmacology, 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

8 authors.

Jianhua DingDepartment of Medical Oncology and Hematology, Gansu Wuwei Tumor Hospital Lanzhou Campus, Gansu Lanzhou, 730000, China. djhhome0322@163.com.
Chai Hong YeongSchool of Medicine, Faculty of Health and Medical Sciences, Taylor's University, Jalan Taylors, Subang Jaya, 47500, Malaysia.
Lei WangDepartment of Medical Oncology and Hematology, Gansu Wuwei Tumor Hospital Lanzhou Campus, Gansu Lanzhou, 730000, China.
Chunyan ShiDepartment of Medical Oncology and Hematology, Gansu Wuwei Tumor Hospital Lanzhou Campus, Gansu Lanzhou, 730000, China.
Long LiDepartment of Medical Oncology and Hematology, Gansu Wuwei Tumor Hospital Lanzhou Campus, Gansu Lanzhou, 730000, China.
Lijun SongDepartment of Hematology, People's Hospital of Ningxia Hui Autonomous Region, Ningxia Medical University, Yinchuan, 750000, Ningxia, China.
Wenxiu MaDepartment of Hematology, Gansu Wuwei Tumor Hospital, Gansu Wuwei, 733000, China.
Peng LiSchool of Computing & Technology, Asia Pacific University of Technology & Innovation, Lebuhraya Bukit Jalil, Taman Teknologi Malaysia, Bukit Jalil, Kuala Lumpur, 57000, Malaysia. 15509519027@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This comprehensive review examines anlotinib, a novel multi-target receptor tyrosine kinase inhibitor with potent antitumor activity. Anlotinib selectively inhibits multiple targets including VEGFR1-3, PDGFR-α, c-Kit, and FGFR1-3, demonstrating superior inhibitory effects compared to other tyrosine kinase inhibitors. The review explores anlotinib’s multifaceted mechanisms of action: inhibition of angiogenesis through disruption of VEGF/PDGF/FGF pathways, suppression of tumor cell migration and invasion via modulation of various signaling cascades, induction of apoptosis through multiple pathways, inhibition of lymphangiogenesis primarily through VEGFR-3 modulation, and positive modulation of the tumor microenvironment. The article further discusses anlotinib’s promising ability to overcome chemoresistance through regulation of drug efflux systems, pro-survival signaling, cancer stemness, and autophagy. The review highlights the synergistic effects of anlotinib in combination therapies with radiochemotherapy, immune checkpoint inhibitors, and targeted drugs across multiple cancer types. Despite its promising efficacy, challenges including low response rates and potential for acquired resistance remain. Future research directions should focus on optimizing dosing regimens, identifying predictive biomarkers, exploring novel combinations, investigating resistance mechanisms, and evaluating anlotinib’s potential in neoadjuvant or adjuvant settings. This extensive analysis provides insights into anlotinib’s therapeutic potential in solid tumors and hematological malignancies, paving the way for more effective and personalized cancer treatment strategies.

Indexed as

Antineoplastic AgentsIndolesNeoplasmsProtein Kinase InhibitorsQuinolinesAnimalsDrug Resistance, NeoplasmHumansTumor MicroenvironmentanlotinibAntineoplastic AgentsIndolesProtein Kinase InhibitorsQuinolinesAnlotinibAnti-angiogenesisCombination therapyDrug resistanceTyrosine kinase inhibitor

Identifiers

PMID40944871

What Socratic holds

Textmetadata
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.