SHU-CHEN WEIPO-NIEN TSAOYu S.-C.Tsai-Wu J.-J.Wu C.H.H.CHIA-TUNG SHUNSu Y.-N.JAU-MIN WONGFON-JOU HSIEH2020-12-222020-12-2220050017-5749https://www.scopus.com/inward/record.uri?eid=2-s2.0-17644379417&doi=10.1136%2fgut.2004.050831&partnerID=40&md5=131d9602b2069400a5995a3ec90ee1e2https://scholars.lib.ntu.edu.tw/handle/123456789/530277Background: Overexpression of vascular endothelial growth factor (VEGF) correlates with vascularity, metastasis, and proliferation in colorectal cancer but the role of its homologue, placenta growth factor (PIGF), is unknown. The aim of this study was to evaluate expression and clinical implications of PIGF in colorectal cancer. Methods: We investigated 74 tumour/non-tumour pairs of colorectal cryosections. Clinical staging was based on the UICC-TNM classification. Expression levels of mRNA for PIGF and VEGF were analysed with quantitative real time reverse transcription-polymerase chain reaction. Proteins were analysed by immunohistochemical staining and enzyme linked immunoabsorbant assay. Analysis of the differences in PIGF and VEGF levels between tumour and non-tumour tissues in the same patient were performed by paired t test; differences between localised and advanced disease patients by the Mann-Whitney, χ2, and Fisher's exact tests and survival curves by the Kaplan-Meier method. Results: Expression levels for both growth factors were significantly higher in tumour than in non-tumour tissues (p?0.001). The ratio of PIGF expression in tumour to non-tumour in the advanced disease group was significantly higher than for the localised disease group (p = 0.009). Patients with more tumour PIGF mRNA had shorter survival (p = 0.028). The majority of PIGF was expressed in tumour cells. Conclusions: Our results suggest that PIGF expression correlates with disease progression and patient survival and may be used as a prognostic indicator for colorectal cancer.[SDGs]SDG3messenger RNA; placental growth factor; vasculotropin; adult; advanced cancer; aged; article; cancer staging; cancer survival; chi square test; colorectal cancer; controlled study; correlation analysis; disease course; enzyme linked immunosorbent assay; evaluation; female; Fisher exact test; gene expression; human; human tissue; immunohistochemistry; Kaplan Meier method; major clinical study; male; priority journal; prognosis; protein analysis; protein expression; protein localization; rank sum test; reverse transcription polymerase chain reaction; survival rate; tissue level; tissue section; tumor cell; Adult; Aged; Aged, 80 and over; Colorectal Neoplasms; Disease Progression; Female; Humans; Immunoenzyme Techniques; Male; Middle Aged; Neoplasm Proteins; Pregnancy Proteins; Prognosis; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; RNA, Neoplasm; Survival Analysis; Tumor Markers, Biological; Up-Regulation; Vascular Endothelial Growth Factorsjournal article10.1136/gut.2004.050831158319132-s2.0-17644379417