Figure 1.
HPV DNA in plasma of patients with cervical cancer. (A) PCR generating 243-bp DNA fragments of HPV E6 gene (B) Dot-blot hybridization for HPV 18 probe Lanes a1-f1 were positive controls using
purified plasmids of HPV type 6, 11, 16, 18, 31 and 33, respectively Lanes a2-f2 were
plasma DNA from patients number 4, 106, 148, 161, 183, and 59 respectively Lanes a3-f3
were tumor DNA from the same patients as lanes a2-f2 (C) PCR generating 1392- and 1028-bp DNA fragments of human PIGR genomic sequence and HPV-18 E2 (D) PCR generating 1026, 1028-bp DNA fragments of HPV 16 and 18 E2 gene, respectively,
from tumor DNA on a 2% agarose gel stained with ethidium bromide (E) Duplex PCR generating 243- and 177-bp DNA fragments of HPV E6 gene and human ZP3 genomic sequence, respectively From left to right of A, C-E: M, 100-bp ladder standard
DNA size marker; - and +, PCR products of the negative control (double-distilled water)
and positive control (Hela cell line for A and E; purified plasmids for D; and for
C, DNA from human leukocyte for PIGR and purified HPV 18 DNA plasmid for E2 gene), respectively; numbers without p indicate
PCR products of tumor DNA; numbers with p indicate PCR products of plasma DNA of CC
patients Number 1061p and 1062p were plasma DNA from patient 106 but the samples were
collected at different time
Pornthanakasem et al. BMC Cancer 2001 1:2 doi:10.1186/1471-2407-1-2 |