SRX852846 GSM1592157 SRP052834 SRS827039 GSM1592157 miRNA-Seq TRANSCRIPTOMIC size fractionation tumor tissue or para-carcinoma tissues were removed, flash frozen on dry ice, and RNA was harvested using Trizol reagent.The 18-30nt fraction of total RNA was excised and purified following 155 Tris-Borate-EDTA denaturing polyacrylamide gel electrophoresis.Before RT-PCR, 5'adaptor and 3'adptor were respectively ligated using T4 RNAligase.Finally, Illumina TruSeq SmallRNA Sample Prep Kit Set D(Cat#RS-200-0048) was used for the construction of sequencing libraries. SmallRNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 GEO Sample GSM1592157 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1592157 gds 301592157 GEO Accession GSM1592157 SRX852847 GSM1592158 SRP052834 SRS827043 GSM1592158 miRNA-Seq TRANSCRIPTOMIC size fractionation tumor tissue or para-carcinoma tissues were removed, flash frozen on dry ice, and RNA was harvested using Trizol reagent.The 18-30nt fraction of total RNA was excised and purified following 155 Tris-Borate-EDTA denaturing polyacrylamide gel electrophoresis.Before RT-PCR, 5'adaptor and 3'adptor were respectively ligated using T4 RNAligase.Finally, Illumina TruSeq SmallRNA Sample Prep Kit Set D(Cat#RS-200-0048) was used for the construction of sequencing libraries. SmallRNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 GEO Sample GSM1592158 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1592158 gds 301592158 GEO Accession GSM1592158 SRX852848 GSM1592159 SRP052834 SRS827040 GSM1592159 miRNA-Seq TRANSCRIPTOMIC size fractionation tumor tissue or para-carcinoma tissues were removed, flash frozen on dry ice, and RNA was harvested using Trizol reagent.The 18-30nt fraction of total RNA was excised and purified following 155 Tris-Borate-EDTA denaturing polyacrylamide gel electrophoresis.Before RT-PCR, 5'adaptor and 3'adptor were respectively ligated using T4 RNAligase.Finally, Illumina TruSeq SmallRNA Sample Prep Kit Set D(Cat#RS-200-0048) was used for the construction of sequencing libraries. SmallRNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 GEO Sample GSM1592159 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1592159 gds 301592159 GEO Accession GSM1592159 SRX852849 GSM1592161 SRP052834 SRS827044 GSM1592161 miRNA-Seq TRANSCRIPTOMIC size fractionation tumor tissue or para-carcinoma tissues were removed, flash frozen on dry ice, and RNA was harvested using Trizol reagent.The 18-30nt fraction of total RNA was excised and purified following 155 Tris-Borate-EDTA denaturing polyacrylamide gel electrophoresis.Before RT-PCR, 5'adaptor and 3'adptor were respectively ligated using T4 RNAligase.Finally, Illumina TruSeq SmallRNA Sample Prep Kit Set D(Cat#RS-200-0048) was used for the construction of sequencing libraries. SmallRNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 GEO Sample GSM1592161 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1592161 gds 301592161 GEO Accession GSM1592161 SRX852850 GSM1592162 SRP052834 SRS827041 GSM1592162 miRNA-Seq TRANSCRIPTOMIC size fractionation tumor tissue or para-carcinoma tissues were removed, flash frozen on dry ice, and RNA was harvested using Trizol reagent.The 18-30nt fraction of total RNA was excised and purified following 155 Tris-Borate-EDTA denaturing polyacrylamide gel electrophoresis.Before RT-PCR, 5'adaptor and 3'adptor were respectively ligated using T4 RNAligase.Finally, Illumina TruSeq SmallRNA Sample Prep Kit Set D(Cat#RS-200-0048) was used for the construction of sequencing libraries. SmallRNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 GEO Sample GSM1592162 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1592162 gds 301592162 GEO Accession GSM1592162 SRX852851 GSM1592163 SRP052834 SRS827042 GSM1592163 miRNA-Seq TRANSCRIPTOMIC size fractionation tumor tissue or para-carcinoma tissues were removed, flash frozen on dry ice, and RNA was harvested using Trizol reagent.The 18-30nt fraction of total RNA was excised and purified following 155 Tris-Borate-EDTA denaturing polyacrylamide gel electrophoresis.Before RT-PCR, 5'adaptor and 3'adptor were respectively ligated using T4 RNAligase.Finally, Illumina TruSeq SmallRNA Sample Prep Kit Set D(Cat#RS-200-0048) was used for the construction of sequencing libraries. SmallRNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 GEO Sample GSM1592163 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1592163 gds 301592163 GEO Accession GSM1592163