Evidence mapPaperPMID 42478378Full record

ReviewTechnology in cancer research & treatment

Leveraging Kinesin Family as Key Regulators of Malignant Progression and the Immunometabolic Niche for Precision Oncology.

Leyi Li, Jing Li, Xinyi Zhao, Haohan Zhang, Qibin Song, Yuchao Dan, Lan Li, Jie Wu, Chao Yang, Junju He and 1 more

Abstract readReview
In one paragraph

Review in Technology in cancer research & treatment. 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
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.

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

11 authors.

Leyi LiCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0009-0000-0455-7365
Jing LiCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0001-5407-840X
Xinyi ZhaoCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0009-0002-3166-6369
Haohan ZhangCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0002-3466-8995
Qibin SongCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0002-4350-0916
Yuchao DanCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0009-0007-2625-143X
Lan LiCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0009-0004-9166-8328
Jie WuCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0003-0935-342X
Chao YangDepartment of Oncology, Affiliated Hospital of Hubei University of Arts and Science, Xiangyang Central Hospital, Xiangyang, China.ORCID 0000-0003-3359-7483
Junju HeCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0001-9147-0996
Bin XuCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0002-0499-0430

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant tumors impose a substantial burden on global health, with an urgent unmet need for effective targets to advance precision therapy. As evolutionarily conserved microtubule motor proteins, the kinesin family (KIF) orchestrates fundamental cellular processes (e.g., intracellular transport, cell division) and canonical signaling pathways, including Wnt and Hippo. Notably, recent studies have uncovered their emerging role in regulating tumor metabolism and reshaping the immune microenvironment, where dysregulated KIF expression drives aberrant tumor proliferation. Based on current research, here we synthesize the latest mechanistic insights into KIF-mediated tumor regulation and evaluate their translational potential as next-generation therapeutic targets and biomarkers for precision cancer therapy. KIF-targeted inhibitors have entered clinical trials across multiple cancer types, holding promise as novel anticancer agents to suppress tumor growth and progression, thereby providing valuable therapeutic options for clinical oncology practice.

Indexed as

KinesinsNeoplasmsPrecision MedicineAnimalsBiomarkers, TumorDisease ProgressionGene Expression Regulation, NeoplasticHumansMetabolic ReprogrammingMolecular Targeted TherapySignal TransductionTumor MicroenvironmentBiomarkers, TumorKinesinsanti-cancer therapy resistancecancer progressionkinesin familymetabolic reprogrammingtumor immune microenvironment

Identifiers

PMID42478378
PMCPMC13389150

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.