Application of circular rnahsa_circ_0008399
A circular and gene expression technology, applied in the field of circular RNA technology research, can solve problems such as unsatisfactory overall survival and progression-free survival of bladder cancer patients
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Embodiment 1
[0105] RNA was extracted from 90 pairs of bladder cancer specimens and their corresponding adjacent normal bladder mucosal epithelial specimens, and then reverse-transcribed and then real-time quantitative PCR (same as above) was performed to detect the expression of circ0008399 in bladder cancer specimens relative to adjacent normal bladder mucosa It can be seen that circ0008399 is highly expressed in bladder cancer specimens. figure 2It shows that the expression level of circ0008399 in bladder cancer clinical tissue samples is higher than that in adjacent normal tissues.
Embodiment 2
[0107] The expression levels of circ0008399 detected in 90 cases of bladder cancer samples carried out in Example 2 were divided into two groups (high and low expression). to the date of death or the last follow-up date of the survivor) to obtain the survival curve, it can be seen that the higher the circ0008399, the shorter the survival time. image 3 It shows that the expression level of circ0008399 is negatively correlated with the survival time of patients.
Embodiment 3
[0109] Two kinds of bladder cancer cells EJ and T24T were seeded in a 6-well plate, and the next day when the density was about 60-80%, the small interfering RNA was transfected to knock down the circ0008399 molecule. The transfection reagent used RNAiMAX (Invitrogen, USA), and the steps were as follows According to the instructions (the ratio of serum-free medium: siRNA: transfection reagent is about 100ul: 2ug: 10ul), the cells were harvested after 24h for RNA extraction, reverse transcription, and real-time quantitative PCR to detect the knockdown efficiency of circ0008399. Figure 4 Verify the efficiency of small interfering RNA knockdown circ0008399.
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