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通过下调Bcl-X(L)诱导失巢凋亡并抑制人卵巢肿瘤在体内的生长。

Induction of anoikis and suppression of human ovarian tumor growth in vivo by down-regulation of Bcl-X(L).

作者信息

Frankel A, Rosen K, Filmus J, Kerbel R S

机构信息

Molecular and Cellular Biology Research, Sunnybrook and Women's College Health Sciences Centre, Department of Laboratory Medicine, University of Toronto, Toronto, Ontario, M4N 3M5 Canada.

出版信息

Cancer Res. 2001 Jun 15;61(12):4837-41.

Abstract

Normal or immortal epithelial cells are sensitive to a form of apoptosis, commonly referred to as anoikis, which is induced by detachment from the extracellular matrix (ECM). In contrast, development of carcinomas is associated with acquisition of cellular resistance to anoikis. However, whether human cancer cells deprived of anoikis resistance necessarily display reduced tumorigenic properties in vivo is unknown. We decided to address this question using human ovarian carcinoma cells as a model. Bcl-X(L), an apoptotic factor considered to play an important role in (resistance to) anoikis, is overexpressed in ovarian cancer, and represents an unfavorable prognostic indicator for this type of human malignancy. We therefore evaluated whether Bcl-X(L) can be used as a tool to manipulate anoikis resistance and tumorigenicity of ovarian cancer cells. We show here that when nonmalignant ovarian epithelial cells are detached from the ECM, down-regulation of Bcl-X(L) and apoptotic cell death are observed, although these events do not occur in ovarian carcinoma cells. Moreover, enforced down-regulation of Bcl-X(L) by transfection with antisense cDNA in the anoikis-resistant and highly tumorigenic HEY ovarian carcinoma cell line had no impact on the viability of these cells under adherent conditions but caused significant apoptosis in response to detachment from the ECM. This change was associated with a strong inhibition of tumorigenicity of the Bcl-X(L)-deficient HEY cells in nude mice, both s.c. and in the peritoneal cavity. These results suggest a critical role for Bcl-X(L) in the maintenance of anoikis resistance in ovarian cancer cells. They also serve to establish a functional linkage between this property and the ability of human cancer cells to grow aggressively in vivo. Consequently, targeting molecular mechanisms responsible for anoikis resistance may serve as a potentially effective therapeutic strategy for the treatment of such human malignancies as ovarian cancer.

摘要

正常上皮细胞或永生上皮细胞对一种通常称为失巢凋亡的细胞凋亡形式敏感,这种凋亡由与细胞外基质(ECM)脱离所诱导。相比之下,癌的发生与细胞获得对失巢凋亡的抗性有关。然而,丧失失巢凋亡抗性的人类癌细胞在体内是否必然表现出降低的致瘤特性尚不清楚。我们决定以人卵巢癌细胞为模型来解决这个问题。Bcl-X(L)是一种被认为在(对)失巢凋亡中起重要作用的凋亡因子,在卵巢癌中过度表达,是这类人类恶性肿瘤的不良预后指标。因此,我们评估了Bcl-X(L)是否可作为一种工具来操控卵巢癌细胞的失巢凋亡抗性和致瘤性。我们在此表明,当非恶性卵巢上皮细胞与ECM脱离时,会观察到Bcl-X(L)的下调和凋亡性细胞死亡,尽管这些事件在卵巢癌细胞中不会发生。此外,在对失巢凋亡具有抗性且高度致瘤的HEY卵巢癌细胞系中,通过反义cDNA转染强制下调Bcl-X(L),对这些细胞在贴壁条件下的活力没有影响,但在细胞从ECM脱离时会导致显著的凋亡。这种变化与Bcl-X(L)缺陷型HEY细胞在裸鼠皮下和腹腔内致瘤性的强烈抑制相关。这些结果表明Bcl-X(L)在维持卵巢癌细胞的失巢凋亡抗性中起关键作用。它们还有助于在这种特性与人类癌细胞在体内侵袭性生长的能力之间建立功能联系。因此,针对负责失巢凋亡抗性的分子机制可能是治疗卵巢癌等人类恶性肿瘤的一种潜在有效治疗策略。

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