AI Article Synopsis

  • HPV (Human Papillomavirus) can keep oral keratinocytes from differentiating, but the reasons for this resistance are not well understood.
  • In a study, researchers examined how different calcium levels affect the growth of HPV16-positive keratinocytes and found that up to a certain calcium level, cell growth increased, while higher levels inhibited it.
  • They observed a significant increase in the expression of the HPV E6 gene at high calcium concentrations, suggesting that HPV16-positive cells can continue to proliferate even when exposed to differentiation signals, which is a key feature of their resilience.

Article Abstract

Human papillomaviruses (HPV) are known to immortalize oral keratinocytes in vitro, but the underlying mechanisms causing the following resistance to differentiation remain unclear. We investigated the effect of extracellular calcium on the proliferation of HPV16-positive keratinocytes and on the mRNA expression of the viral E6-oncogene. HPV16-positive hypopharyngeal carcinoma cells (UD-SCC-2), spontaneously immortalized- (HMK) and HPV16 E6/E7-immortalized human gingival keratinocytes (IHGK) were grown for 3, 6 and 9 days in Keratinocyte Serum-free Medium with calcium concentrations ranging from 0 mM to 6 mM. Calcium concentrations up to 0.09 mM increased cellular proliferation, which decreased at higher concentrations. A shift of calcium concentration from 0 to 4 mM increased E6 expression in UD-SCC-2 cells 2.4-fold by day 9. Simultaneously, E2 expression increased. The most significant upregulation of E6 and E2 expressions was observed at day 9, grown in high-calcium media and the increase in E6 expression coincided with an increase in involucrin expression, likely indicating cell differentiation. Despite this, HPV-positive cells continued to proliferate even at high-calcium media in contrast to HPV-negative cells. Overexpression of E6 mRNA may be an important feature of HPV16-positive cells to resist the natural calcium gradient in differentiating keratinocytes allowing cell proliferation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282442PMC
http://dx.doi.org/10.1111/apm.12227DOI Listing

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