Downregulation of nucleophosmin expression inhibited proliferation and induced apoptosis in salivary gland adenoid cystic carcinoma

J Oral Pathol Med. 2017 Mar;46(3):175-181. doi: 10.1111/jop.12482. Epub 2016 Aug 8.

Abstract

Background: This study aimed to explore the relationship between nucleophosmin (NPM1) and patient clinical characteristics. Moreover, we investigated the effect of NPM1 in tumor proliferation and apoptosis of salivary gland adenoid cystic carcinoma (SACC).

Materials and methods: NPM1 expression was examined in 74 specimens of SACC and 31 non-cancerous epithelium adjacent to carcinoma (NCEAC) by immunohistochemistry (IHC). RNA interference technology was used to silence NPM1 expression in SACC cells. We used transwell culture assay, cell counting kit-8 tests, and colony formation assay to test the proliferation, cisplatin resistance, migration, and invasiveness of SACC cells.

Results: The nuclear and cytoplasmic expression of NPM1 in SACC tissue was overexpressed and was tightly linked to perineural invasion and lymph node metastasis. The downregulation of NPM1 inhibited proliferation and induced apoptosis in SACC cells. Knockdown of NPM1 expression had no effect on chemoresistance migration, or invasiveness.

Conclusions: NPM1 may play an important role in tumor progress in SACC and is a potential biomarker for SACC.

Keywords: invasiveness; migration; nucleophosmin; proliferation; salivary adenoid cystic carcinoma.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Apoptosis / physiology*
  • Biomarkers, Tumor / metabolism*
  • Carcinoma, Adenoid Cystic / metabolism*
  • Carcinoma, Adenoid Cystic / physiopathology
  • Cell Line, Tumor
  • Cell Proliferation
  • Down-Regulation
  • Female
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Nuclear Proteins / metabolism*
  • Nucleophosmin
  • RNA Interference
  • Salivary Gland Neoplasms / metabolism*
  • Salivary Gland Neoplasms / physiopathology

Substances

  • Biomarkers, Tumor
  • NPM1 protein, human
  • Nuclear Proteins
  • Nucleophosmin