[No authors listed]
Lowâdensity lipoprotein receptorârelated protein 6 (LRP6) promotes metastasis in numerous types of cancer; however, its role in trophoblast cells has been less frequently reported. In the present study, the effects of upâ and downregulation of LRP6 on trophoblast cells were investigated accordingly. The study aimed to develop a therapeutic target for gestational choriocarcinoma. The expression levels of LRP6 in preâeclampsia (PE) tissues, trophoblast cell lines and gestational choriocarcinoma cells were determined using reverse transcriptionâquantitative polymerase chain reaction (RTâqPCR) assay. Doubleâluciferase reporter analysis was conducted to detect the regulatory gene of LRP6. Furthermore, the proliferative, migratory and invasive abilities of trophoblasts and gestational choriocarcinoma cells were determined by CCKâ8, wound healing, and Transwell assays, respectively. The expression levels of the genes and proteins of interest [matrix metalloproteinase (MMP)â2, MMPâ9, tissue inhibitor of metalloproteinaseâ1 (TIMPâ1), and TIMPâ2] associated with tumor cell invasion were measured by performing RTâqPCR and western blotting, respectively. The National Center for Biotechnology Information database revealed that LRP6 was relatively highly expressed in placental tissues, but was poorly expressed in PE tissues and trophoblast cell lines. The upregulation of LRP6 not only increased the activity, migration and invasion of trophoblast cells, but it also promoted the expression of MMPâ2 and MMPâ9, whereas it inhibited the expression levels of TIMPâ1 and TIMPâ2. Such results followed the opposite trend to those of downregulation of LRP6 in gestational choriocarcinoma cells. Moreover, LRP6 was predicted to be the target gene for microRNA (miR)â346, which was highly expressed in PE tissues and trophoblast cell lines. The present study also revealed that LRP6 could reverse the effects of miRâ346 on the proliferation, migration and invasion of trophoblast cells. Therefore, considered collectively, the results of the present study have demonstrated that LRP6 is involved in the proliferation, migration and invasion of trophoblast cells via miRâ346, and that LRP6 may serve as a potential target in cancer treatment.
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