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. Author manuscript; available in PMC: 2009 Jul 2.
Published in final edited form as: J Invest Dermatol. 2008 Jun 12;128(12):2888–2893. doi: 10.1038/jid.2008.162

Table 3.

Previous Studies of β-HPV DNA detection in NMSC tumor samples of immunocompetent individuals

Author (year) Sample size Methods1 β-HPV types detected Main findings
Forslund et al. (2007) 82 SCCs
126 BCCs
Single and nested PCR of L1 region using CP65/CP70 and FAP primers2 8, 9, 12, 14, 15, 19, 20, 21, 23, 24, 37, 38, 80, 93, 96 Association between β-species 2 and SCC
Pfister et al. (2003) 20 SCCs Nested PCR of L1 region using CP62/CP70a and CP65/CP69a primers 5, 8, 12, 14, 15, 19, 21, 24, 25, 37, 38 80% of AK and 40% of SCC lesions were positive for βHPV DNA
Iftner et al. (2003) 72 SCCs
18 BCCs
PCR of E1 region using CP4/CP5 and PPF1/CP5 primers 5, 8, 12, 17, 19, 22, 36 Association between β-HPV DNA and NMSC (OR 6.4)
Boxman et al. (2000) 14 BCCs Nested PCR of the L1 region using CP62/CP70a and CP65/CP69a primers 5, 8, 12, 14, 15, 17, 25,37, 38 43% of BCC tumors were β-HPV DNA-positive
Surentheran et al. (1998) 6 SCCs Degenerate and nested PCR of the L1 region using HPV2/B5, F14/B15, MY09/11, CP62/69 5, 8, 19, 20, 21, 23, 36 All SCC samples were negative most likely due to low viral copy number

AK, actinic keratoses; BCC, basal cell carcinoma; CI, confidence interval; HPV, human papillomavirus; NMSC, non-melanoma skin cancer; OR, odds ratio; SCC, squamous cell carcinoma

1

All PCR-based methods were followed by direct sequencing.

2

Pooled results from three laboratories using different PCR methods.