ELK Foundation for Health Research, An Scoil Monzaird, Crieff, Scotland, PH7 4JT, U.K.
Anticancer Res. 2013 Sep;33(9):3611-4.
Expression of human chorionic gonadotropin beta subunit (hCGβ) by epithelial carcinomas is associated with a poor prognosis and has a proposed autocrine growth effect on cancer cells by inhibition of apoptosis.
We transduced the hCGβ-expressing bladder cancer cell line SCaBER with short hairpin (sh) RNA lentiviral gene-specific (CGB) constructs and determined its impact on the synthesis of hCGβ and the resultant effect on cancer cell growth.
Stable CGB gene-silenced clones exhibited a 60%-80% reduction in the level of hCGβ expressed and a reduced growth rate of more than 40% compared to wild-type SCaBER cells.
shRNA Lentiviral particles achieve stable knockdown of hCGβ translation in the bladder cancer cell line SCaBER. This transforms the phenotype by reducing hCGβ expression and cell growth rate. This is consistent with the proposed autocrine/paracrine function of ectopic hCGβ expression during oncogenesis.
人绒毛膜促性腺激素β亚单位(hCGβ)在癌上皮细胞中的表达与预后不良有关,并通过抑制细胞凋亡对癌细胞具有拟内分泌生长作用。
我们用短发夹(sh)RNA 慢病毒基因特异性(CGB)构建物转导 hCGβ 表达的膀胱癌细胞系 SCaBER,并测定其对 hCGβ 合成的影响以及对癌细胞生长的影响。
与野生型 SCaBER 细胞相比,稳定的 CGB 基因沉默克隆表现出 hCGβ 表达水平降低 60%-80%,生长速度降低超过 40%。
shRNA 慢病毒颗粒可在膀胱癌细胞系 SCaBER 中实现 hCGβ 翻译的稳定敲低。这通过降低 hCGβ 表达和细胞生长速率来改变表型。这与在肿瘤发生过程中异位 hCGβ 表达的自分泌/旁分泌功能一致。