Sieving and checking method for cancers
A technology for screening, cancer, applied in the field of medical molecular biology
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Embodiment 1
[0067] Embodiment one material and method
[0068] 1. Test materials
[0069] The test materials included a series of complete samples of cervical lesions, including normal samples (n=45), low-grade squamous cell intraepithelial lesions (LSIL, n=45), high-grade squamous cell intraepithelial lesions (HSIL, n=58 ), squamous cell carcinoma (squamous cell carcinoma, SCC, n=109); the test materials also included a series of complete ovarian tumor samples, including ovarian benign tumor samples (n=36), ovarian borderline tumor samples (n=6 ), ovarian cancer samples (n=122); all cervical samples and ovarian samples were obtained from the Gynecological Tumor Tissue Bank of Taipei Tri-Service General Hospital. The DNA was quantified by the method, and the quality of the DNA was checked by gel electrophoresis.
[0070] In addition, the liver cell samples include normal liver cell samples (n=13), chronic hepatitis (n=15), liver cirrhosis (cirrhosis, n=40), liver cancer (hepatocellular ...
Embodiment 2
[0095] Example 2 Screening of cervical cancer methylation indicator genes
[0096]Using CpG island microarrays (CpG island microarrays) to carry out differential methylation heterozygous reaction (DMH) to screen out genes with high methylation in cervical squamous cell carcinoma (SCC); CpG island microarrays ( CpG island microarrays) showed that there were 216 sites with differential methylation between cervical cancer tissue samples and normal Pap smear samples. After removing sequence repeats, 26 gene activating sub-region CpG islands were obtained ( promoter CGIs).
[0097] These gene activators were sequenced and analyzed, and 6 genes were selected, including: SOX1 (SEQ ID No: 1), PAX1 (SEQ ID No: 2), LMX1A (SEQ ID No: 3), NKX6 -1 (SEQ ID No: 4), WT1 (SEQ ID No: 5) and ONECUT1 (SEQ ID No: 6), the details of which are shown in Table 4; as can be seen from Table 4, these six genes are all developing Important transcription factors (transcription factors) in the process, SO...
Embodiment 3
[0103] Example 3 Correlation between DNA methylation and gene expression in cervical cancer cell lines
[0104] In order to confirm whether the expression of cervical cancer methylation pointer genes is regulated by DNA methylation, DNA methyltransferase inhibitor 5'-aza-2'-deoxycytidine (AZC) (Sigma Chemical Co. ) to treat the HeLa cervical cancer cell line for 4 days, and then check the demethylation of the above six gene activators by methylation-specific PCR (MSP); Primer (U), and the MSP primer (M) that can specifically identify methylated gene sequences for methylation-specific PCR (MSP), the results are as follows Figure 4A As shown, in the HeLa cervical cancer cell line (AZC-) not treated with 5'-aza-2'-deoxycytidine (AZC), all six target genes had methylation phenomenon (such as Figure 4A shown in column 1), and unmethylated genes (such as Figure 4A Shown in column 2); while in HeLa cervical cancer cell lines (AZC+) treated with 5'-aza-2'-deoxycytidine (AZC) for ...
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