Down-regulation of long non-coding RNA markers in lung cancer and its application
A long-chain non-coding, marker technology, applied in the field of lung cancer down-regulating long-chain non-coding RNA markers, can solve problems such as lung damage, existing risks, sensitivity and specificity need to be improved, and achieve high accuracy and sensitivity. high effect
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Embodiment 1
[0040] Example 1: Diagnostic markers for lung cancer:
[0041] The present invention provides 21 types of lung cancer markers, which can be used alone or in combination of two or more to diagnose lung cancer; including: AC010776.2, AC027277.2, AC091588.3, AC093110.1, AC135178 .1, AL024497.2, AL109741.1, AL136369.1, AL355499.1, AL359378.1, AL589935.1, AP001528.2, CLIC5, FENDRR, FO393415.1, LINC00472, LINC00968, LINC01290, PCAT19, TBX2- , TMEM51-AS1; its nucleotide probe sequence is shown in Table 1.
[0042] Table 1. Nucleotide probe sequences of 21 markers
[0043] landmark Nucleotide Probe Sequence AC010776.2 ATGTGGTGAGCTCGCCTGAAGACTTCAGACACGGGTCCACGTGTGTCCCAACGCCAGGAG AC027277.2 ATATTTGACACCATGATTGTCCTGAGAAATCTAGGATGCAAAATCGCCATCACCATGCAG AC091588.3 AAACATCTCTTTCAAAATAAAGGCACGAGAATCACGTTCTGTCAGCGCAGTCGCCACTGT AC093110.1 ATTAATCCAAGATGTACAGTGGAGTTTGTCTACAGAGACACTGACATGACTTCTGAAGCC AC135178.1 TGACTTTGTGGAAGCGCAGCCTTTGGGTGAGCCGG...
Embodiment 2
[0044] Example 2: Screening and identification of diagnostic markers for lung cancer
[0045] In the present invention, gene chips or real-time fluorescent quantitative PCR methods are used to screen and identify markers, but the identification is not necessarily limited to the above methods, and other methods such as chemical analysis methods are also suitable for screening and identification of markers. In the present invention, lung tissue is taken as an example to illustrate the screening and identification of markers:
[0046] 1. Obtain subject samples and perform pretreatment:
[0047] Lung tumor tissues and normal lung tissues of 23 patients with lung cancer were surgically extracted, and total RNA in tissue blocks or cells was extracted using Trizol (Invitrogen, USA). and further adopt The RNA clean-up kit (Macherey Nagel, Germany) was used to purify the total RNA through a column. Quantification was then performed by spectrophotometric methods and integrity was c...
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