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Cancer Res. 2019 Sep 1;79(17):4480-4490. doi: 10.1158/0008-5472.CAN-19-0384. Epub 2019 Jun 25.
2
The Role of PPAR-δ in Metabolism, Inflammation, and Cancer: Many Characters of a Critical Transcription Factor.过氧化物酶体增殖物激活受体-δ(PPAR-δ)在代谢、炎症和癌症中的作用:作为关键转录因子的多面性。
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3
Tumor Heterogeneity in Primary Colorectal Cancer and Corresponding Metastases. Does the Apple Fall Far From the Tree?原发性结直肠癌及其相应转移灶中的肿瘤异质性。子代会与亲代差异很大吗?
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4
Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.全球癌症统计数据 2018:GLOBOCAN 对全球 185 个国家/地区 36 种癌症的发病率和死亡率的估计。
CA Cancer J Clin. 2018 Nov;68(6):394-424. doi: 10.3322/caac.21492. Epub 2018 Sep 12.
5
Peroxisome proliferator-activated receptor γ coactivator-1α is a predictor of lymph node metastasis and poor prognosis in human colorectal cancer.过氧化物酶体增殖物激活受体γ共激活因子-1α是人类结直肠癌淋巴结转移和预后不良的一个预测指标。
Ann Diagn Pathol. 2018 Apr;33:11-16. doi: 10.1016/j.anndiagpath.2017.11.007. Epub 2017 Nov 10.
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Correction to: The role of pparγ and autophagy in ros production, lipid droplets biogenesis and its involvement with colorectal cancer cells modulation.对《过氧化物酶体增殖物激活受体γ和自噬在活性氧生成、脂滴生物合成及其与结肠癌细胞调节的关系中的作用》的更正
Cancer Cell Int. 2017 Nov 2;17:99. doi: 10.1186/s12935-017-0463-1. eCollection 2017.
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Activation of PPARα by clofibrate sensitizes pancreatic cancer cells to radiation through the Wnt/β-catenin pathway.氯贝酸酯激活 PPARα 通过 Wnt/β-catenin 通路使胰腺癌细胞对辐射敏感。
Oncogene. 2018 Feb 15;37(7):953-962. doi: 10.1038/onc.2017.401. Epub 2017 Oct 23.
8
Peroxisome proliferator-activated receptors (PPARs) are potential drug targets for cancer therapy.过氧化物酶体增殖物激活受体(PPARs)是癌症治疗的潜在药物靶点。
Oncotarget. 2017 Jul 27;8(36):60704-60709. doi: 10.18632/oncotarget.19610. eCollection 2017 Sep 1.
9
Peroxisome Proliferator-Activated Receptor Gamma in Obesity and Colorectal Cancer: the Role of Epigenetics.过氧化物酶体增殖物激活受体 γ 在肥胖与结直肠癌中的作用:表观遗传学视角。
Sci Rep. 2017 Sep 6;7(1):10714. doi: 10.1038/s41598-017-11180-6.
10
Cytotoxic effect of a family of peroxisome proliferator-activated receptor antagonists in colorectal and pancreatic cancer cell lines.一类过氧化物酶体增殖物激活受体拮抗剂对结肠癌细胞系和胰腺癌细胞系的细胞毒性作用。
Chem Biol Drug Des. 2017 Nov;90(5):1029-1035. doi: 10.1111/cbdd.13026. Epub 2017 Jul 19.

过氧化物酶体增殖物激活受体在结直肠癌中的异常表达及其与癌症进展和预后的关系。

Aberrant Expression of Peroxisome Proliferator-Activated Receptors in Colorectal Cancer and Their Association with Cancer Progression and Prognosis.

作者信息

Yaghoubizadeh Musa, Pishkar Leila, Basati Gholam

机构信息

Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Department of Biology, Islamshahr Branch, Islamic Azad University, Islamshahr, Iran.

出版信息

Gastrointest Tumors. 2020 Apr;7(1-2):11-20. doi: 10.1159/000503995. Epub 2019 Nov 1.

DOI:10.1159/000503995
PMID:32399461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7206611/
Abstract

INTRODUCTION

Peroxisome proliferator-activated receptors (PPARs), PPARα, PPARγ, and PPARδ, are nuclear ligand-activated transcription factors which presumably contribute to a broad range of pathophysiological processes, such as tumorigenesis. Nevertheless, their exact role as tumor suppressors or promoters is not straightforward in colorectal cancer (CRC). Therefore, expression values of these PPARs and their relation with tumor progression and prognosis were examined in CRC patients.

METHODS

In this work, the relative expression values of the PPARs were measured by real-time polymerase chain reaction in 100 CRC tumor tissues paired with adjacent normal tissues. After that, the association between relative expression values of the PPARs in tumor tissues and the cancer progression-related clinicopathological characteristics as well as overall survival of patients were assessed.

RESULTS

While PPARα and PPARδ seemed to be overexpressed, PPARγ was suppressed in CRC tumor tissues compared with paired adjacent normal tissues ( = 0.0001). The relative expressions of PPARα and PPARδ were negatively associated with tumor size, tumor grade, TNM stage, metastasis, lymphatic invasion, and decreased overall survival time ( < 0.05). The same associations, but in reverse direction, were found for PPARγ.

CONCLUSIONS

It was found that PPARα and PPARδ were overexpressed while PPARγ was suppressed in CRC tumor tissues, and these deregulations are associated with cancer progression and poor prognosis.

摘要

引言

过氧化物酶体增殖物激活受体(PPARs),即PPARα、PPARγ和PPARδ,是核配体激活的转录因子,可能参与广泛的病理生理过程,如肿瘤发生。然而,它们在结直肠癌(CRC)中作为肿瘤抑制因子或促进因子的确切作用并不明确。因此,本研究检测了CRC患者中这些PPARs的表达值及其与肿瘤进展和预后的关系。

方法

在本研究中,通过实时聚合酶链反应检测了100例CRC肿瘤组织及其配对的相邻正常组织中PPARs的相对表达值。之后,评估肿瘤组织中PPARs的相对表达值与癌症进展相关的临床病理特征以及患者总生存期之间的关联。

结果

与配对的相邻正常组织相比,CRC肿瘤组织中PPARα和PPARδ似乎过表达,而PPARγ受到抑制( = 0.0001)。PPARα和PPARδ的相对表达与肿瘤大小、肿瘤分级、TNM分期、转移、淋巴浸润以及总生存时间缩短呈负相关( < 0.05)。PPARγ则呈现相反的关联。

结论

研究发现,CRC肿瘤组织中PPARα和PPARδ过表达,而PPARγ受到抑制,这些失调与癌症进展和不良预后相关。