Target intelligence / Profile preview

Kinesin family member C2 (KIFC2)

Target
KIFC2
Molecular classification
Motor protein, Microtubule motor protein, Kinesin superfamily protein
01

Overview

Kinesin family member C2 (KIFC2) is a member of the kinesin-14 subfamily of microtubule-based motor proteins, with C-terminal motor domains and high specificity for neural tissues. It is primarily involved in microtubule-dependent organelle transport within neurons, playing a potential role in retrograde axonal and dendritic transport of multivesicular bodies. Recent studies have identified a novel role for KIFC2 in cancer biology—specifically, in hormone receptor-positive, HER2-negative breast cancer—where KIFC2 stabilizes cyclin-dependent kinase 4 (CDK4), promoting cell proliferation and contributing to resistance against endocrine therapy and CDK4/6 inhibitors. KIFC2 can therefore serve as both a potential therapeutic target and a biomarker predicting therapeutic resistance. High expression in tumors is associated with poor prognosis. While it is largely dispensable for normal development in mice, its neural enrichment and involvement in vesicle transport highlight the need for caution if targeting it therapeutically[1][2][3][4][5].

Other names
Kinesin-like protein KIFC2KIFC2
02

Mechanism of action

For drugs: Sensitization to antimetabolites and CDK4/6 inhibitors by reducing KIFC2 activity, which destabilizes CDK4 and disrupts cell cycle progression[1][5].

03

Biological functions

Microtubule-dependent organelle transportRetrograde axonal transportRegulation of cell cycle progression (via CDK4 stabilization)Potential role in mitotic spindle assembly
04

Disease associations

Cancer (notably hormone receptor-positive, HER2-negative breast cancer)Possibly other cancers (prostate cancer, colon adenocarcinoma) as a prognostic biomarker
05

Safety considerations

Not specifically reported; KIFC2 itself appears non-essential for viability in mice (based on knockout studies), but therapeutic targeting may require assessment of neuronal function since KIFC2 is enriched in neural tissues[4].
06

Interacting drugs

Capecitabine (increased sensitivity when KIFC2 is overexpressed)

2 more in the full profile.

07

Biomarkers

High KIFC2 expression predicts poor prognosis and therapeutic resistance in hormone receptor-positive, HER2-negative breast cancer[1][5].

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