Application of CircHOMER1 and colorectal cancer treatment preparation
A colorectal cancer and preparation technology, applied in the field of tumor molecular biology, can solve the problems of circRNA function without research reports, etc., achieve the results of authentic and reliable results, rigorous test process, and improve the effect of treatment efficacy
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Embodiment 1
[0052] Example 1: RNA-seq experiment
[0053] RNA-Seq sequencing was performed on the cells before and after PDT treatment, and the differentially expressed circRNAs after PDT treatment were screened. This part of the experiment was completed by Guangzhou Ruibo Biotechnology Co., Ltd. The specific steps are as follows: After RNA extraction and quality inspection, the rRNA was removed by the probe, and the linear RNA was removed by RNaseR to construct the Illumina sequencing library. Sequencing was then performed, the sequencing mode was PE150, and the sequencing data volume was 12G / 15G. For the sequencing data, first perform Raw Data filtering, de-joining sequences and low-quality reads to obtain high-quality data (Clean Data). Then, by comparing with the ribosome database, the ribosomal RNA sequence is removed to obtain valid reads. Valid reads are compared with the reference genome (mapping), and the comparison results are used for the identification of circular RNAs in th...
Embodiment 2
[0058] Example 2: qPCR detection of expression of circular RNA circHOMER1 in colorectal cancer tissue
[0059] 40 pairs of fresh tissues were collected for qPCR to detect the expression of circular RNA circHOMER1 in colorectal cancer and adjacent tissues. The results are as follows: image 3 shown. Circular RNA circHOMER1 was highly expressed in paracancerous tissues and low in colorectal cancer tissues.
Embodiment 3
[0060] Example 3: qPCR detection of the expression of circular RNA circHOMER1 after photodynamic treatment
[0061] After colorectal cancer cells RKO and CX-1 were incubated with complete medium (containing 0.1 μM photosensitizer) for 4 hours, 10 cm 2 / J laser treatment. After continuing to culture for 6 hours, the cells were collected and Trizol was added to lyse the cells and the expression of circular RNA circHOMER1 was detected.
[0062] The expression levels of circular RNA circHOMER1 in RKO, RKO-PDT and CX-1, CX-1-PDT group cells were detected by qPCR. Such as Figure 4 As shown, the expression level of circular RNA circHOMER1 was significantly upregulated in RKO and CX-1 cells after photodynamic treatment.
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