# Functional roles of Keratin 6A in disease pathogenesis across cancer and skin disorders

**Authors:** Yanyan Su, Shudong Su, Min Li, Zhixia Zhang, Shiyi Zhang, Caixia Fan, Wei Luo, Shuming Guo

PMC · DOI: 10.3389/ebm.2026.10845 · Experimental Biology and Medicine · 2026-01-21

## TL;DR

Keratin 6A (KRT6A) plays a key role in cancer progression and skin disorders, influencing tumor growth, treatment resistance, and disease pathology.

## Contribution

This paper systematically reviews KRT6A's functional roles in cancer and skin diseases, highlighting its potential as a therapeutic target.

## Key findings

- KRT6A promotes tumor progression through epithelial-mesenchymal transition and immune evasion.
- Elevated KRT6A is linked to resistance to chemotherapy, targeted therapy, and radiotherapy.
- KRT6A mutations cause pachyonychia congenita and contribute to psoriasis.

## Abstract

Keratin 6A (KRT6A) is an epithelial-specific type II keratin localized within cytoskeletal intermediate filaments and functions in cooperation with KRT16/17 to maintain epidermal homeostasis and tissue repair. Accumulating evidence highlights its multifaceted roles in cancer. Aberrant KRT6A expression promotes cell cycle progression, epithelial–mesenchymal transition, migration, and invasion, thereby driving tumor initiation and metastasis, although tumor-suppressive effects have been observed in specific contexts. Mechanistically, KRT6A regulates adhesion, cytoskeletal remodeling, and critical signaling pathways, thereby reshaping tumor immunity and metabolism to facilitate immune evasion and metabolic dysregulation. Elevated KRT6A expression is strongly associated with resistance to chemotherapy, targeted therapy, and radiotherapy. Therapeutic approaches targeting KRT6A include nucleic acid-based interventions, protein degradation strategies, inhibition of upstream regulatory pathways, and combinatorial regimens to overcome drug resistance. Clinically, KRT6A has emerged as both a diagnostic and prognostic biomarker, supporting treatment monitoring and enhancing predictive models for risk stratification and individualized outcome evaluation. Beyond oncology, mutations in KRT6A underlie pachyonychia congenita, and its dysregulation contributes to epidermal hyperproliferative disorders such as psoriasis. Overall, systematic elucidation of the structure–function–pathway–clinical axis of KRT6A offers new opportunities for precision medicine and supports its potential as a therapeutic target in cancer management.

## Linked entities

- **Genes:** KRT6A (keratin 6A) [NCBI Gene 3853], KRT16 (keratin 16) [NCBI Gene 3868], KRT17 (keratin 17) [NCBI Gene 3872]
- **Diseases:** pachyonychia congenita (MONDO:0016471), psoriasis (MONDO:0005083)

## Full-text entities

- **Genes:** KRT80 (keratin 80) [NCBI Gene 144501] {aka KB20}, KRT6A (keratin 6A) [NCBI Gene 3853] {aka CK-6C, CK-6E, CK6A, CK6C, CK6D, K6A}
- **Diseases:** skin disorders (MESH:D012871), metabolic dysregulation (MESH:D021081), cancer (MESH:D009369), psoriasis (MESH:D011565), pachyonychia congenita (MESH:D053549), epidermal hyperproliferative disorders (MESH:D004814), metastasis (MESH:D009362)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12867935/full.md

## References

115 references — full list in the complete paper: https://tomesphere.com/paper/PMC12867935/full.md

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Source: https://tomesphere.com/paper/PMC12867935