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Cytokeratin-8 in anaplastic thyroid carcinoma: More than a simple structural cytoskeletal protein

  • Dehuang Guo
    ,
  • Qinqin Xu
    ,
  • Sarabjot Pabla
    ,
  • John Koomen
    ,
  • Paul Williams Biddinger
    ,
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Research
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Anaplastic thyroid carcinoma (ATC) is almost universally fatal. Elevated keratin-8 (KRT8) protein expression is an established diagnostic cancer biomarker in several epithelial cancers (but not ATC). Several keratins, including KRT8, have been suggested to have a role in cell biology beyond that of structural cytoskeletal proteins. Here, we provide evidence that KRT8 plays a direct role in the growth of ATCs. Genomic and transcriptomic analysis of >5000 patients demonstrates that KRT8 mutation and copy number amplification are frequently evident in epithelial-derived cancers. Carcinomas arising from diverse tissues exhibit KRT8 mRNA and protein overexpression when compared to normal tissue levels. Similarly, in a panel of patient-derived ATC cell lines and patient tumors, KRT8 expression shows a similar pattern. sh-RNA-mediated KRT8 knockdown in these cell lines increases apoptosis, whereas forced overexpression of KRT8 confers resistance to apoptosis under peroxide-induced cell stress conditions. We further show that KRT8 protein binds to annexin A2, a protein known to mediate apoptosis as well as the redox pathway.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Research
Peer-review

Original language

English (US)

Article number

577

Journal (Volume, Issue Number)

International journal of molecular sciences (Volume 19, Issue 2)

Publication milestones

  • Published - 02/14/2018

Publication status

Published - 02/14/2018

ISSN

1661-6596

Publication IDs

  • Scopus: 85042208740
  • PubMed: 29443941
  • ORCID: /0000-0001-9597-4374/work/54990721

Publication metrics

Metrics

SciVal
citations
4
SciVal
FWCI
0.40
SciVal
Author count
15
SciVal
Paper percentile
62
Fractional count
5
Fractional count
0.33
Fractional count
10
Fractional count
0.67
Fractional count
5
Fractional count
1
Scopus
citations

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Citation count
17
Captures
25

Funding Details

The authors would like to thank Nita Maihle and William David Hill for review of this manuscript, the Augusta University Electron Microscopy and Histology Core for assistance with tissue microarray (TMA) slide sectioning, the National Cancer Institute, American Academy of Otolaryngology/Head and Neck Surgery and American Head and Neck Society who provided funding (PMW) that enabled early progress leading to this study. This study was internally funded by the corresponding author’s institutional startup funds (PMW) and by the Ministry of Science and Technology grants MOST-103-2320-B-007-005 and MOST-104-2320-B-007-002 (CCC). Acknowledgments: The authors would like to thank Nita Maihle and William David Hill for review of this manuscript, the Augusta University Electron Microscopy and Histology Core for assistance with tissue microarray (TMA) slide sectioning, the National Cancer Institute, American Academy of Otolaryngology/Head and Neck Surgery and American Head and Neck Society who provided funding (PMW) that enabled early progress leading to this study. This study was internally funded by the corresponding author’s institutional startup funds (PMW) and by the Ministry of Science and Technology grants MOST-103-2320-B-007-005 and MOST-104-2320-B-007-002 (CCC).
FundersFunding numbers
American Academy of Otolaryngology/Head
-
CCC
-
Core
-
Ministry of Science and Technology
MOST-103-2320-B-007-005, MOST-104-2320-B-007-002
PMW
-
NCI
-
AAO-HNS
-