Quantification of nucleic acid quality in postmortem tissues from a cancer research autopsy program

被引:16
|
作者
Fan, Jun [1 ]
Khanin, Raya [2 ]
Sakamoto, Hitomi [1 ]
Zhong, Yi [1 ]
Michael, Chelsea [3 ]
Pena, Derwin [3 ]
Javier, Breanna [1 ]
Wood, Laura D. [6 ]
Iacobuzio-Donahue, Christine A. [3 ,4 ,5 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Bioinformat Core, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10065 USA
[4] Mem Sloan Kettering Canc Ctr, Human Oncol & Pathogenesis Program, New York, NY 10065 USA
[5] Mem Sloan Kettering Canc Ctr, David M Rubenstein Ctr Pancreat Canc Res, New York, NY 10065 USA
[6] Johns Hopkins Univ, Sch Med, Dept Pathol, Sol Goldman Pancreat Canc Res Ctr, Baltimore, MD 21231 USA
基金
美国国家卫生研究院;
关键词
autopsy; RNA; post-mortem; RNA sequencing; metastasis; GENE-EXPRESSION; PANCREATIC-CANCER; CLINICAL RESISTANCE; METASTASIS; INHIBITION; COMPLEXITY; LANDSCAPE; MARKERS;
D O I
10.18632/oncotarget.11836
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The last decade has seen a marked rise in the use of cancer tissues obtained from research autopsies. Such resources have been invaluable for studying cancer evolution or the mechanisms of therapeutic resistance to targeted therapies. Degradation of biomolecules is a potential challenge to usage of cancer tissues obtained in the post-mortem setting and remains incompletely studied. We analysed the nucleic acid quality in 371 different frozen tissue samples collected from 80 patients who underwent a research autopsy, including eight normal tissue types, primary and metastatic tumors. Our results indicate that RNA integrity number (RIN) of normal tissues decline with the elongation of post-mortem interval (PMI) in a tissue-type specific manner. Unlike normal tissues, the RNA quality of cancer tissues is highly variable with respect to post-mortem interval. The kinetics of DNA damage also has tissue type-specific features. Moreover, while DNA degradation is an indicator of low RNA quality, the converse is not true. Finally, we show that despite RIN values as low as 5.0, robust data can be obtained by RNA sequencing that reliably discriminates expression signatures.
引用
收藏
页码:66906 / 66921
页数:16
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