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Rampant centrosome amplification underlies more aggressive disease course of triple negative breast cancers

机译:猖cent的中心体扩增是三阴性乳腺癌的更具侵略性的疾病过程的基础

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摘要

Centrosome amplification (CA), a cell-biological trait, characterizes pre-neoplastic and pre-invasive lesions and is associated with tumor aggressiveness. Recent studies suggest that CA leads to malignant transformation and promotes invasion in mammary epithelial cells. Triple negative breast cancer (TNBC), a histologically-aggressive subtype shows high recurrence, metastases, and mortality rates. Since TNBC and non-TNBC follow variable kinetics of metastatic progression, they constitute a novel test bed to explore if severity and nature of CA can distinguish them apart. We quantitatively assessed structural and numerical centrosomal aberrations for each patient sample in a large-cohort of grade-matched TNBC (n = 30) and non-TNBC (n = 98) cases employing multi-color confocal imaging. Our data establish differences in incidence and severity of CA between TNBC and non-TNBC cell lines and clinical specimens. We found strong correlation between CA and aggressiveness markers associated with metastasis in 20 pairs of grade-matched TNBC and non-TNBC specimens (p < 0.02). Time-lapse imaging of MDA-MB-231 cells harboring amplified centrosomes demonstrated enhanced migratory ability. Our study bridges a vital knowledge gap by pinpointing that CA underlies breast cancer aggressiveness. This previously unrecognized organellar inequality at the centrosome level may allow early-risk prediction and explain higher tumor aggressiveness and mortality rates in TNBC patients.
机译:中心体扩增(CA)是一种细胞生物学特征,具有肿瘤形成前和浸润前病变的特征,并与肿瘤侵袭性相关。最近的研究表明,CA导致恶性转化并促进乳腺上皮细胞的侵袭。在组织学上具有攻击性的三阴性乳腺癌(TNBC)显示高复发,转移和死亡率。由于TNBC和非TNBC遵循可变的转移进程动力学,因此它们构成了一种新颖的试验床,以探讨CA的严重程度和性质是否可以区分它们。我们使用多色共聚焦成像技术对一大批等级匹配的TNBC(n = 30)和非TNBC(n = 98)病例中每个患者样品的结构和数值中心像差进行了定量评估。我们的数据建立了TNBC和非TNBC细胞系和临床标本之间CA发病率和严重程度的差异。我们在20对等级匹配的TNBC和非TNBC标本中发现CA和与转移相关的侵袭性标记之间有很强的相关性(p <0.02)。包含扩增的中心体的MDA-MB-231细胞的延时成像显示出增强的迁移能力。我们的研究通过指出CA是乳腺癌侵略性的基础,弥合了重要的知识鸿沟。这种先前无法识别的中心体细胞器不平等可能允许早期风险预测,并可以解释TNBC患者较高的肿瘤侵袭性和死亡率。

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