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pmid:32922552

TMT-labeling Proteomics of Papillary Thyroid Carcinoma Reveal Invasive Biomarkers.

Jiaqi Dai · Xiaqing Yu · Yali Han · Li Chai · Yina Liao · Peng Zhong · Ruting Xie · Xuechen Sun · Qingqing Huang · Jian Wang · Zhiqiang Yin · Yun Zhang · Zhongwei Lv · Chengyou Jia

Journal of Cancer · 2020 doi:10.7150/jca.47290

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
TMT-labeling Proteomics of Papillary Thyroid Carcinoma Reveal Invasive Biomarkers.
doi
10.7150/jca.47290
pmid
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Jiaqi Dai
[1]
Xiaqing Yu
[2]
Yali Han
[3]
Li Chai
[4]
Yina Liao
[5]
Peng Zhong
[6]
Ruting Xie
[7]
Xuechen Sun
[8]
Qingqing Huang
[9]
Jian Wang
[10]
Zhiqiang Yin
[11]
Yun Zhang
[12]
Zhongwei Lv
[13]
Chengyou Jia
journal
Journal of Cancer
year
2020
abstract
Background and Aim: Invasion and metastasis are critical events in papillary thyroid carcinoma (PTC) progression. Protein markers specific to this process may avoid over-treatment and urgently needed. Methods: TMT-labeled mass spectrometry-based proteomics were carried out on PTC and invasive phenotype (iPTC) (3 pairs per group) and cross validate differentially expressed proteins (DEPs) (FC>1.5 and <0.67 and p<0.05) with GEO and TCGA datasets and the correlation genes of DEPs were also analyzed. Results: We identified and quantified 4607 proteins identical to PTC and iPTC groups. Among which 12 DEPs in PTC and 179 DEPs in iPTCs were found. Cross-validation with GSE60542 and TCGA database revealed 10 DEPs that all significant correlated with metastasis and staging. Upregulated SLC27A6 showed negative correlation with 6 out of 9 downregulated DEPs including HGD, CA4, COL23A1, SLC26A7, FHL1 and TPO. Conclusion: The panel of 7 genes (SLC27A6 and 6 downregulated DEPs) could have ideal prediction value to improve our understanding of invasiveness of PTC.
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To validate whether the DEPs were consistent at mRNA level and genomic level, we also analyzed GEO datasets using the GPL570 platform which included 11 PTC samples from N0 (no lymph node metastasis) and 13 from N+ (with lymph node metastasis) patients (GEO dataset: GSE60542) .
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To validate whether the DEPs were consistent at mRNA level and genomic level, we also analyzed GEO datasets using the GPL570 platform which included 11 PTC samples from N0 (no lymph node metastasis) and 13 from N+ (with lymph node metastasis) patients (GEO dataset: GSE60542) .
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Revisiting the transcriptional analysis of primary tumors and associated nodal metastases with enhanced biological and statistical controls: application to thyroid cancer
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To validate whether the DEPs were consistent at mRNA level and genomic level, we also analyzed GEO datasets using the GPL570 platform which included 11 PTC samples from N0 (no lymph node metastasis) and 13 from N+ (with lymph node metastasis) patients (GEO dataset: GSE60542) .
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TMT-labeling Proteomics of Papillary Thyroid Carcinoma Reveal Invasi
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Methods: TMT-labeled mass spectrometry-based proteomics were carried out on PTC and invasive phenoty
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nt and urgently needed. Methods: TMT-labeled mass spectrometry-based proteomics were carried out on PTC and
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