Yaghoubizadeh Musa, Pishkar Leila, Basati Gholam
Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Department of Biology, Islamshahr Branch, Islamic Azad University, Islamshahr, Iran.
Gastrointest Tumors. 2020 Apr;7(1-2):11-20. doi: 10.1159/000503995. Epub 2019 Nov 1.
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.
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.
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.
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.
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。
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。
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。
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。