The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Pan-Cancer
Peroxisome proliferator-activated receptors (PPARs) are members of nuclear transcription factors. The functions of the PPAR family (PPARA, PPARD, and PPARG) and their coactivators (PPARGC1A and PPARGC1B) in maintenance of lipid and glucose homeostasis have been unveiled. However, the roles of PPARs...
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doaj-93a29415013c47b087baab72910138252020-11-25T03:58:13ZengHindawi LimitedPPAR Research1687-47571687-47652020-01-01202010.1155/2020/65275646527564The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Pan-CancerRunzhi Huang0Jiaqi Zhang1Mingxiao Li2Penghui Yan3Huabin Yin4Suna Zhai5Xiaolong Zhu6Peng Hu7Jiaxin Zhang8Ling Huang9Man Li10Zehui Sun11Tong Meng12Daoke Yang13Zongqiang Huang14Department of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaDepartment of Orthopedics, Shanghai General Hospital, School of Medicine, Shanghai Jiaotong University, 100 Haining Road, Shanghai, ChinaDepartment of Radiotherpy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, ChinaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaDepartment of Orthopedics, Shanghai General Hospital, School of Medicine, Shanghai Jiaotong University, 100 Haining Road, Shanghai, ChinaDepartment of Radiotherpy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, ChinaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, 1 East Jianshe Road, Zhengzhou, ChinaPeroxisome proliferator-activated receptors (PPARs) are members of nuclear transcription factors. The functions of the PPAR family (PPARA, PPARD, and PPARG) and their coactivators (PPARGC1A and PPARGC1B) in maintenance of lipid and glucose homeostasis have been unveiled. However, the roles of PPARs in cancer development remain elusive. In this work, we made use of 11,057 samples across 33 TCGA tumor types to analyze the relationship between PPAR transcriptional expression and tumorigenesis as well as drug sensitivity. We performed multidimensional analyses on PPARA, PPARG, PPARD, PPARGC1A, and PPARGC1B, including differential expression analysis in pan-cancer, immune subtype analysis, clinical analysis, tumor purity analysis, stemness correlation analysis, and drug responses. PPARs and their coactivators expressed differently in different types of cancers, in different immune subtypes. This analysis reveals various expression patterns of the PPAR family at a level of pan-cancer and provides new clues for the therapeutic strategies of cancer.http://dx.doi.org/10.1155/2020/6527564 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Runzhi Huang Jiaqi Zhang Mingxiao Li Penghui Yan Huabin Yin Suna Zhai Xiaolong Zhu Peng Hu Jiaxin Zhang Ling Huang Man Li Zehui Sun Tong Meng Daoke Yang Zongqiang Huang |
spellingShingle |
Runzhi Huang Jiaqi Zhang Mingxiao Li Penghui Yan Huabin Yin Suna Zhai Xiaolong Zhu Peng Hu Jiaxin Zhang Ling Huang Man Li Zehui Sun Tong Meng Daoke Yang Zongqiang Huang The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Pan-Cancer PPAR Research |
author_facet |
Runzhi Huang Jiaqi Zhang Mingxiao Li Penghui Yan Huabin Yin Suna Zhai Xiaolong Zhu Peng Hu Jiaxin Zhang Ling Huang Man Li Zehui Sun Tong Meng Daoke Yang Zongqiang Huang |
author_sort |
Runzhi Huang |
title |
The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Pan-Cancer |
title_short |
The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Pan-Cancer |
title_full |
The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Pan-Cancer |
title_fullStr |
The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Pan-Cancer |
title_full_unstemmed |
The Role of Peroxisome Proliferator-Activated Receptors (PPARs) in Pan-Cancer |
title_sort |
role of peroxisome proliferator-activated receptors (ppars) in pan-cancer |
publisher |
Hindawi Limited |
series |
PPAR Research |
issn |
1687-4757 1687-4765 |
publishDate |
2020-01-01 |
description |
Peroxisome proliferator-activated receptors (PPARs) are members of nuclear transcription factors. The functions of the PPAR family (PPARA, PPARD, and PPARG) and their coactivators (PPARGC1A and PPARGC1B) in maintenance of lipid and glucose homeostasis have been unveiled. However, the roles of PPARs in cancer development remain elusive. In this work, we made use of 11,057 samples across 33 TCGA tumor types to analyze the relationship between PPAR transcriptional expression and tumorigenesis as well as drug sensitivity. We performed multidimensional analyses on PPARA, PPARG, PPARD, PPARGC1A, and PPARGC1B, including differential expression analysis in pan-cancer, immune subtype analysis, clinical analysis, tumor purity analysis, stemness correlation analysis, and drug responses. PPARs and their coactivators expressed differently in different types of cancers, in different immune subtypes. This analysis reveals various expression patterns of the PPAR family at a level of pan-cancer and provides new clues for the therapeutic strategies of cancer. |
url |
http://dx.doi.org/10.1155/2020/6527564 |
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