1 / 1

Triage of Women with ASCUS and ASC-H Cytology by PAX1 Methylation

Triage of Women with ASCUS and ASC-H Cytology by PAX1 Methylation. XIV-029. 1 . 三軍總醫院病理部暨國防醫學院病理研究所 2 . 三軍總醫院婦產部 柯鋒翌 * 1 、 賴鴻政 # 2 、 趙載光 # 1. Background. Results. PAX1 methylation test. Follow -up Histology. Previous Cytology. N=56.

lihua
Download Presentation

Triage of Women with ASCUS and ASC-H Cytology by PAX1 Methylation

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Triage of Women with ASCUS and ASC-H Cytology by PAX1 Methylation XIV-029 1.三軍總醫院病理部暨國防醫學院病理研究所 2.三軍總醫院婦產部 柯鋒翌*1、賴鴻政#2、趙載光#1 Background Results PAX1 methylation test Follow -up Histology Previous Cytology N=56 The identification of a small percentage of carcinoma in situ (CIS) among patients with minor cytological abnormalities (atypical squamous cells of undetermined significance [ASCUS] or atypical squamous cells cannot exclude HSIL [ASC-H] group) is a major problem in cytology-based cervical cancer screening. Here we investigated the efficacy of PAX1 methylation as a biomarker to identify samples of patients with CIS among those with an ASCUS or ASC-H result in Papanicolaou cytology. Follow-up diagnosis TestResult A B (+)=7 (-)=49 (+)=1 Reactive Change (-)=49 ASCUS ASCUS (+)=6 Carcinoma In situ C D (-)=0 Sensitivity =100% Specificity = 98% E F Materials and Methods Conclusion Consecutive liquid-based cytology specimens of 40 ASCUS and 10 ASC-H results were selected from gynecologists who subsequent follow-up with biopsy or repeat smear 6 months later, independent of the PAX1 result. Genomic DNA was extracted from liquid-based smears and then treat with bisulfite to converse non-methylation cytosine. After that we use real-time polymerase chain reaction (PCR) to detect PAX1 and COL2A1. To measure of gene methylation we calculated the “percentage of methylated reference” (PMR) for each real-time PCR result using Ct values for the PAX1 gene and a control COL2A1 gene. CIS These data suggested that the use of PAX1 methylation state as a biomarker in cervical cytology to triage ASCUS and ASC-H cases allows identification of CIS with good sensitivity and specificity. Fig.1 (A)cytology diagnosis with ASCUS. (B)Normal cervical epithelial (C) cytology diagnosis with ASC-H. (D)Squamous metaplasia. (E)Carcinoma in situ . (F) Carcinoma in situ. References ASC-H ASCUS • Gynecologic Oncology 2003, 91:201-208. • 2.Cancer Cytopathol 2004; 102:100-108. • 3.Cancer Cytopathol 2007;111:58–66. • 4.Int. J. Cancer: 2008;123, 161–167 . CIS Reactive change CIS Reactive change 5 1 10 Case number 40

More Related