High Expression of NEK2 and PIM1, but Not PIM3, Is Linked to an Aggressive Phenotype of Bronchopulmonary Neuroendocrine Neoplasms

Endocr Pathol. 2020 Sep;31(3):264-273. doi: 10.1007/s12022-020-09629-y.

Abstract

Dysregulations of the NEK2 and PIM1-3 kinase signaling axes have been implicated in the pathogenesis of several cancers, including those with a neuroendocrine phenotype. However, their impact on bronchopulmonary neuroendocrine neoplasms (BP-NENs) has not been investigated. The aim of this pilot study was to determine mRNA and protein levels of NEK2, PIM1, and PIM3 in a group of 49 patients with BP-NENs: 11 typical carcinoids, 5 atypical carcinoids, 11 large cell neuroendocrine carcinomas, 22 small cell lung carcinomas (SCLC). The expression was measured using TaqMan-based RT-PCR and immunohistochemistry. NEK2 and PIM1 mRNA levels were higher in the SCLC patients than in the other BP-NEN groups (p < 0.001). There was an association between NEK2 mRNA and protein expression (p = 0.023) and elevated NEK2 mRNA levels were related to reduced survival in BP-NEN patients (p = 0.015). Patients with higher PIM1 protein expression had also diminished survival comparing with those with weak or no PIM1 expression (p = 0.037). Elevated NEK2 and PIM1 expression were related to aggressive tumor phenotype and indirectly affected the overall survival of BP-NEN patients. Our pilot study supports the need for future investigation of the biological function of NEK2 and PIM1 in BP-NEN transformation to verify the clinical value of our findings.

Keywords: Bronchopulmonary neuroendocrine neoplasm; Expression; NEK2; PIM1; PIM3.

MeSH terms

  • Aged
  • Biomarkers, Tumor / genetics
  • Carcinoma, Neuroendocrine / diagnosis
  • Carcinoma, Neuroendocrine / genetics
  • Carcinoma, Neuroendocrine / pathology*
  • Cohort Studies
  • Disease Progression
  • Female
  • Gene Expression Regulation, Neoplastic
  • Genetic Association Studies
  • Humans
  • Lung Neoplasms / diagnosis
  • Lung Neoplasms / genetics
  • Lung Neoplasms / pathology*
  • Male
  • Middle Aged
  • NIMA-Related Kinases / genetics*
  • Neoplasm Invasiveness
  • Neuroendocrine Tumors / diagnosis
  • Neuroendocrine Tumors / genetics
  • Neuroendocrine Tumors / pathology*
  • Phenotype
  • Pilot Projects
  • Protein Serine-Threonine Kinases / genetics*
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogene Proteins c-pim-1 / genetics*

Substances

  • Biomarkers, Tumor
  • Proto-Oncogene Proteins
  • NEK2 protein, human
  • NIMA-Related Kinases
  • PIM1 protein, human
  • PIM3 protein, human
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-pim-1