CDK14 expression is elevated in patients with non-small cell lung cancer and correlated with poor prognosis

J Int Med Res. 2021 Oct;49(10):3000605211013199. doi: 10.1177/03000605211013199.

Abstract

Objective: To investigate the clinical significance of cyclin-dependent kinase 14 (CDK14) expression in patients with non-small cell lung cancer (NSCLC).

Methods: The present prospective observational study included 193 patients diagnosed with NSCLC between January 2010 and December 2014. NSCLC tumor tissues and paired paracancerous normal tissues were obtained from all patients. CDK14, thyroid transcription factor 1 (TTF-1), cytokeratin 5/6 (CK5/6), and Ki67 expression was measured via immunohistochemistry (IHC).

Results: CDK14 staining was strong (>3) in 129 patients (66.49%) and weak (≤3) in 64 patients (33.16%). The mean IHC scores were markedly higher in tumor tissues than in paracancerous tissues. Pearson's analysis demonstrated that the IHC scores of CDK14 expression were positively correlated with TTF-1, CK5/6, and Ki67 scores. Kaplan-Meier analysis illustrated that 5-year overall survival was markedly longer in patients with weak CDK14 staining. TNM stage, pleural invasion, lymph node metastasis, CDK14 expression, and Ki67 expression were risk factors for 5-year overall survival in patients with NSCLC.

Conclusion: CDK14 overexpression portended poor outcomes in patients with NSCLC, and CDK14 expression was correlated with TTF-1, CK5/5, and Ki67 expression.

Keywords: Cyclin-dependent kinase 14; Ki67; cytokeratin 5/6; immunohistochemistry; non-small cell lung cancer; overall survival; prognosis; thyroid transcription factor 1.

Publication types

  • Observational Study
  • Retracted Publication

MeSH terms

  • Carcinoma, Non-Small-Cell Lung* / diagnosis
  • Carcinoma, Non-Small-Cell Lung* / genetics
  • Cyclin-Dependent Kinases
  • Humans
  • Immunohistochemistry
  • Lung Neoplasms* / diagnosis
  • Lung Neoplasms* / genetics
  • Lymphatic Metastasis
  • Prognosis

Substances

  • CDK14 protein, human
  • Cyclin-Dependent Kinases