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Open AccessJournal ArticleDOI

PDZ and LIM domain protein 1(PDLIM1)/CLP36 promotes breast cancer cell migration, invasion and metastasis through interaction with α-actinin

TLDR
It is shown here that CLP36 is critical for promoting breast cancer cell migration and invasion in vitro and metastasis in vivo, whereas it is dispensable for breast cell proliferation and anchorage-independent growth in vitroand tumor growth in vivo.
Abstract
Increased CLP36 expression has been found to be closely associated with breast cancer progression. However, whether and how it contributes to malignant behavior of breast cancer cells were not known. We show here that CLP36 is critical for promoting breast cancer cell migration and invasion in vitro and metastasis in vivo, whereas it is dispensable for breast cell proliferation and anchorage-independent growth in vitro and tumor growth in vivo. CLP36 interacted with both α-actinin-1 and -4 in breast cancer cells. Depletion of either α-actinin-1 or -4 inhibited breast cancer cell migration. Furthermore, mutations inhibiting the α-actinin-binding activity abolished the ability of CLP36 to promote breast cancer cell migration. Finally, depletion of CLP36 or disruption of the CLP36-α-actinin complex in breast cancer cells substantially inhibited Cdc42 activation, cell polarization and migration. Our results identify CLP36 as an important regulator of breast cancer cell migration and metastasis, and shed light on how increased CLP36 expression contributes to the progression of breast cancer.

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Upregulation of hsa_circ_0136666 contributes to breast cancer progression by sponging miR-1299 and targeting CDK6.

TL;DR: It was revealed that Upregulation of hsa_circ_0136666 promoted breast cancer progression by sponging miR‐1299 and targeting CDK6.
Journal ArticleDOI

Meta-analysis of gene expression studies in endometrial cancer identifies gene expression profiles associated with aggressive disease and patient outcome.

TL;DR: The value of employing meta-analysis to improve the power of gene expression microarray data is demonstrated, and genes and molecular pathways of importance for endometrial cancer therapy are highlighted.
Journal ArticleDOI

PDLIM5 inhibits STUB1-mediated degradation of SMAD3 and promotes the migration and invasion of lung cancer cells.

TL;DR: It is shown that the scaffolding protein PDLIM5 (PDZ and LIM domain protein 5, ENH) critically promotes TGFβ signaling by maintaining SMad3 stability in NSCLC and is a novel regulator of basal SMAD3 stability.
Journal ArticleDOI

Active FOXO1 Is a Key Determinant of Isoform-Specific Progesterone Receptor Transactivation and Senescence Programming

TL;DR: This study indicates FOXO1 as a critical component for progesterone signaling to promote cellular senescence and reveals a novel mechanism for transcription factor control of hormone sensitivity.
References
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Journal ArticleDOI

Rho GTPases Control Polarity, Protrusion, and Adhesion during Cell Movement

TL;DR: It is concluded that the signal transduction pathways controlled by the four small GTPases, Rho, Rac, Cdc42, and Ras, cooperate to promote cell movement.
Journal ArticleDOI

Cdc42 - the centre of polarity

TL;DR: It is now clear that many features of the molecular mechanisms controlling polarization are conserved in all eukaryotic cells, including Cdc42, a small GTPase of the Rho family.
Journal ArticleDOI

Rho GTPases are over‐expressed in human tumors

TL;DR: Overall, increase in the amount of Rho GTPases, in particular RhoA, appears to be a frequent event in different types of human tumors, which supports the view that RhoGTPases are involved in human carcinogenesis.
Journal ArticleDOI

Molecular mechanisms of invadopodium formation the role of the N-WASP–Arp2/3 complex pathway and cofilin

TL;DR: Results indicate that EGF receptor signaling regulatesInvadopodium formation through the N-WASP–Arp2/3 pathway and cofilin is necessary for the stabilization and maturation of invadopodia.
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