Application of cFAM210A in preparation of kit and drug for liver cancer diagnosis or postoperative prediction
A technology for diagnostic kits and diagnostic reagents, applied in the directions of drug combination, recombinant DNA technology, DNA/RNA fragments, etc., can solve the problem that the occurrence and development mechanism has not yet been reported, and achieves a simple detection method, and improves the detection rate and accuracy. , the effect of short cycle
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Embodiment 1
[0043] Example 1: Validation of the ring structure of cFAM210A
[0044] 1.1 Extraction of total RNA from liver tissue
[0045] Take a mung bean-sized liver tissue, add an appropriate amount (usually 1mL) of RNAiso Plus and homogenate; let stand at room temperature for 5 minutes, then centrifuge at 12000g / min, 4°C for 5 minutes; transfer the supernatant to a new 1.5mL EP tube , discard the precipitate; add 0.2 times the volume of RNAiso Plus (usually 0.2mL) of chloroform, shake and mix, and let stand at room temperature for 5 minutes; centrifuge at 12000g / min, 4°C for 15 minutes, and transfer the supernatant to Add an equal volume of isopropanol to a new 1.5mLEP tube, let stand at room temperature for 10 minutes; centrifuge at 12000g / min, 4°C for 10 minutes (white precipitate can be seen at the bottom of the tube), discard the liquid, keep the precipitate, add RNAiso Plus, etc. A volume (usually 1ml) of 75% ethanol was centrifuged at 7500g / min at 4°C for 5 minutes, the liquid ...
Embodiment 2
[0065] Example 2 Detection of the expression level of cFAM210A in liver cancer and adjacent tissues
[0066] 1. Sample collection
[0067] 80 pairs of liver cancer and paracancerous tissue samples were collected and placed in a -80°C refrigerator. All cases did not receive radiotherapy and chemotherapy before surgery, all patients signed informed consent, and the experimental protocol was approved by the ethics committee of the unit.
[0068] The extraction, reverse transcription and real-time quantitative PCR of liver tissue RNA are as described in Example 1. By detecting the expression of cFAM210A in 80 pairs of liver cancer and adjacent tissues, it was found that the expression of cFAM210A in liver cancer tissues was significantly lower than that of adjacent tissues ( figure 2 A, Wilcoxon signed-rank test, P<0.001). The effect of cFAM210A expression in liver tissue in diagnosing liver cancer is expressed as 0.751 (0.677-0.826) by the area under the ROC curve (receiver o...
Embodiment 3
[0069] Example 3 The predictive effect of cFAM210A on the prognosis of patients with liver cancer
[0070] The extraction, reverse transcription and real-time quantitative PCR of liver tissue RNA are as described in Example 1. We detected the expression of cFAM210A in 80 pairs of liver cancer and adjacent tissues, and found that the overall survival rate of liver cancer patients with low cFAM210A expression was significantly lower than that of liver cancer patients with high cFAM210A expression ( image 3 A, Log-rank, P=0.019), the recurrence-free survival rate of liver cancer patients with low expression of cFAM210A was also significantly lower than that of liver cancer patients with high expression of cFAM210A ( image 3 B, Log-rank, P=0.031).
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