RAB22A-NoeFs fusion gene system for diagnosing and/or treating osteosarcoma, and application thereof
A technology of rab22a-noefs and rab22a-noef1, applied in the field of RAB22A-NoeFs fusion gene line, can solve the problems of inability to evaluate clinical value and significance, achieve the effect of inhibiting migration and invasion, inhibiting lung metastasis, and promoting lung metastasis
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Embodiment 1
[0039] Example 1 Identification of RAB22A-NoeFs fusion gene sequence
[0040] Using RNA-seq, the RAB22A-NoeFs fusion gene was found in the human osteosarcoma cell lines ZOS and ZOSM. Subsequently, the full length of the CDS region of the RAB22A-NoeFs fusion gene was amplified to verify the obtained RAB22A-NoeFs fusion gene. The specific process is as follows:
[0041] 1. High-throughput sequencing identification of fusion genes in osteosarcoma cells:
[0042] Select primary osteosarcoma cells ZOS, osteosarcoma cell line ZOSM, and normal bone cells Hfob1.19, extract total RNA with TRIZOL, and send to Beijing Nuohezhiyuan Bioinformation Technology Co., Ltd. for library building and high-throughput second-generation transcriptome After sequencing and bioinformatics analysis, the RAB22A-NoeFs fusion gene was specifically expressed in the primary osteosarcoma cells ZOS and ZOSM (Table 1); the schematic diagram of the fusion method of the RAB22A-NoeFs fusion gene is shown in figu...
Embodiment 2
[0058] Example 2 Detection of RAB22A-NoeFs fusion gene
[0059] 1. RT-PCR detection
[0060]Extract the RNA of osteosarcoma cells ZOS, ZOSM and normal osteoblast Hhob1.19, reverse transcribe into cDNA; use the cDNA as a template, perform PCR verification on the RAB22A-NoeFs fusion gene, and perform Sanger sequencing on the PCR product; including the following steps:
[0061] (1) Design and screen specific RT-PCR primers, specific RT-PCR primers are as follows:
[0062] RAB22A-NoeFs-F: GGCCTCTCCCCTTCTCAACTTAG (SEQ ID NO: 13)
[0063] RAB22A-NoeF1-R: GTGGCTTTCTCAGCCGAAAC (SEQ ID NO: 14)
[0064] RAB22A-NoeF2-R: TCATTGATAGGCATCTGGGTTGGTT (SEQ ID NO: 15)
[0065] RAB22A-NoeF3-R: TCAGCCTCTAAGGTAGCTAGGACAA (SEQ ID NO: 16)
[0066] RAB22A-NoeF4-R: TCACCTGAGGTCAGGAGTTCGAGAC (SEQ ID NO: 17)
[0067] RAB22A-NoeF5-R: TTAGGTCATGTGCCCATATCTGAAC (SEQ ID NO: 18)
[0068] RAB22A-NoeF6-R: CTAAATCGATATTCCAATCTGGTCT (SEQ ID NO: 19)
[0069] (2) Trizol method to extract RNA
[0070] Add 1...
Embodiment 3
[0093] Example 3 Function of RAB22A-NoeFs fusion gene in osteosarcoma
[0094] 1. Construction of stable overexpression cells
[0095] 1. Construction of overexpression vector
[0096] (1) CDS region sequence amplification of RAB22A-NoeFs
[0097] Using TAKARA's high-fidelity enzyme MIX primSTAR, the specific primers in Example 2 were used to amplify the CDS region sequence of RAB22A-NoeFs. The system is as follows:
[0098]
[0099] Place it in a PCR instrument after mixing it evenly, and the reaction conditions are as follows:
[0100] After pre-denaturation at 95°C for 5 minutes, carry out 38 cycles under the following conditions:
[0101] 98°C 15s
[0102] 55-60℃ 30s
[0103] 72℃ 5kb / min
[0104] After 38 cycles, a further step of 72°C, 10min extension reaction was performed, after which the amplified product was recovered;
[0105] (2) Digestion (including overexpression vector PBABE and amplification products)
[0106] Perform digestion reactions in 200 μL PCR...
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