Application of c22orf41 as a tumor marker in pancreatic cancer
A tumor marker, pancreatic cancer technology, applied in the field of genetic engineering, can solve problems such as difficulty in early diagnosis, and achieve far-reaching clinical significance.
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Embodiment 1
[0030] Example 1 Survival analysis of pancreatic cancer based on TCGA database information Screening related genes
[0031] 1. Screening of clinical information
[0032] The clinical information of pancreatic cancer patients in the TCGA database was retrieved. As of December 10, 2015, a total of 185 clinical cases of pancreatic cancer were recorded in the TCGA database. These data were screened, and a total of 160 patients were included in the study. Patients with medical history of other malignancies, who had received radiotherapy or chemotherapy were excluded during screening, and patients included in the study were required to contain clinical information and mRNA data.
[0033] 2. Survival study sample statistics
[0034] The statistical results of the survival time of 160 patients with pancreatic cancer are shown in the following table:
[0035] Table 1 Survival time statistics of 160 patients with pancreatic cancer
[0036]
[0037] 3. Research plan for survival a...
Embodiment 2
[0043] Example 2 RT-PCR Detection of the Expression of Gene C22orf41 in Pancreatic Cancer and Paracancerous Tissues
[0044] 1. Materials
[0045] 1.1 Histopathological specimens
[0046] Tissues from 20 patients with pancreatic cancer who underwent surgical resection and were confirmed by pathological examination and corresponding paracancerous tissue samples were collected. Paracancerous tissue was defined as pancreatic tissue beyond 3 cm from the tumor edge. The samples were collected from patients who were diagnosed with pancreatic cancer and underwent surgical resection at Peking Union Medical College Hospital from October 2014 to December 2016. Immediately after surgical resection of pancreatic cancer tissue, under the guidance of pathologists, pancreatic cancer and paracancerous tissues were taken and placed in liquid nitrogen, and stored in a -80°C low-temperature refrigerator after serial numbering.
[0047] 1.2 The inclusion criteria are as follows:
[0048] (1) C...
Embodiment 3
[0078] Example 3 Effect of silencing C22orf41 expression on the proliferation of pancreatic cancer cells
[0079] 1. Design of shRNA sequence
[0080]For the target gene sequence of the target gene, use the RNA interference sequence design principles provided on the Pubmed website to design multiple RNA interference target sequences, and perform evaluation and determination based on relevant design experience and design software. The siRNA of the three RNA interference target sequences, simultaneously Select the scramble sequence recognized in RNAi design as a control, and the sequence is shown in Table 3: the scramble sequence is shown in SEQ ID NO.5, the target sequence of interference 1 is shown in SEQ ID NO.6, and the target sequence of interference 2 is shown in SEQ ID As shown in NO.7, the target sequence of interference 3 is shown in SEQ ID NO.8. According to the characteristics of the pLKO.1-TRC cloning vector, the DNA sequence of the siRNA and its corresponding compl...
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