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Status |
Public on Oct 20, 2020 |
Title |
FAM83H-AS1 is a non-coding oncogenic driver and therapeutic target of lung adenocarcinoma |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Our study suggested that FAM83H-AS1 was a potential oncogenic driver due to chromosome 8q24 amplification in lung adenocarcinoma. To investigate the molecular mechanism of FAM83H-AS1, we performed high-thoughput RNA sequencing (RNA-Seq) assays after the silence of FAM83H-AS1 in A549 cell lines.
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Overall design |
In human lung adenocarcinoma A549 cells, we downregulated the expression of FAM83H-AS1 utilizing small interference RNA (siRNA) and used scrumble as negative control. Then we used RNA-Seq to reveal the change of mRNA profiles after the silence of FAM83H-AS1.
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Contributor(s) |
Wang S, Ma Z, Xia W, Qiu M, Yin R |
Citation(s) |
33634993 |
Submission date |
Oct 19, 2020 |
Last update date |
Feb 27, 2021 |
Contact name |
Rong Yin |
E-mail(s) |
rong_yin@njmu.edu.cn
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Organization name |
Nanjing Medical University Affiliated Jiangsu Cancer Hospital
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Department |
Thoracic Surgery
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Street address |
Baiziting 42
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City |
Nanjing |
ZIP/Postal code |
210009 |
Country |
China |
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Platforms (1) |
GPL17303 |
Ion Torrent Proton (Homo sapiens) |
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Samples (6)
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Relations |
BioProject |
PRJNA669700 |
SRA |
SRP287504 |