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分散因子在体外影响前列腺上皮细胞集落在骨髓基质上的形成。

Scatter factor influences the formation of prostate epithelial cell colonies on bone marrow stroma in vitro.

作者信息

Lang S H, Clarke N W, George N J, Testa N G

机构信息

CRC Section of Haemopoietic Cell and Gene Therapeutics, Patterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester, UK.

出版信息

Clin Exp Metastasis. 1999 Jun;17(4):333-40. doi: 10.1023/a:1006696002497.

Abstract

Prostate cancer metastases form selectively in the bone marrow. Previously we demonstrated motility was important for the formation of primary prostatic epithelial cell colonies in bone marrow stroma (BMS) co-culture. In this study we looked at the influence of motility factors on the colony formation of epithelial cells derived from benign (bPEC) or malignant (mPEC) prostate tissue. After 7 days co-culture we found that anti-scatter factor consistently inhibited prostate epithelial cell colony formation on BMS (7/7 mPEC and 4/7 bPEC samples showed significant inhibition). Antibodies against bFGF and 5T4 did not significantly affect colony formation. Addition of fibroblast conditioned media (derived from benign prostates) to co-cultures stimulated the colony formation of bPEC (170%) and mPEC (252%). This stimulation was eliminated by depletion of SF from the conditioned media. Immunohistochemical staining found c-Met expression in 5/6 bPEC cultures and 7/9 mPEC cultures. When grown in BMS co-culture expression of c-Met was positive in 3/6 bPEC and 2/7 mPEC samples. In conclusion, scatter factor influences the in vitro formation of prostate epithelial cell colonies on BMS co-culture.

摘要

前列腺癌转移灶选择性地在骨髓中形成。此前我们证明,运动性对于骨髓基质(BMS)共培养体系中原发性前列腺上皮细胞集落的形成很重要。在本研究中,我们观察了运动性因子对源自良性(bPEC)或恶性(mPEC)前列腺组织的上皮细胞集落形成的影响。共培养7天后,我们发现抗散射因子持续抑制BMS上前列腺上皮细胞集落的形成(7/7的mPEC样本和4/7的bPEC样本显示出显著抑制)。抗bFGF和5T4的抗体对集落形成没有显著影响。向共培养体系中添加成纤维细胞条件培养基(源自良性前列腺)可刺激bPEC(170%)和mPEC(252%)的集落形成。从条件培养基中去除SF可消除这种刺激作用。免疫组织化学染色发现,5/6的bPEC培养物和7/9的mPEC培养物中有c-Met表达。在BMS共培养体系中生长时,3/6的bPEC样本和2/7的mPEC样本中c-Met表达呈阳性。总之,散射因子影响BMS共培养体系中前列腺上皮细胞集落的体外形成。

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