Connexin 43 mediated gap junctional communication enhances breast tumor cell diapedesis in culture (Q24810763)

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English	Connexin 43 mediated gap junctional communication enhances breast tumor cell diapedesis in culture	scientific article

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instance of

scholarly article

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title

Connexin 43 mediated gap junctional communication enhances breast tumor cell diapedesis in culture (English)

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main subject

breast neoplasm

1 reference

based on heuristic

inferred from title

author

Dale W Laird

object named as

Dale W Laird

series ordinal

3

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author name string

Mary-Ann Pollmann

series ordinal

1

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Qing Shao

series ordinal

2

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Martin Sandig

series ordinal

4

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language of work or name

English

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publication date

2005

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published in

Breast Cancer Research

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volume

7

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issue

4

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page(s)

R522-34

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cites work

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Connexin 26 induces growth suppression, apoptosis and increased efficacy of doxorubicin in prostate cancer cells

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Retroviral delivery of connexin genes to human breast tumor cells inhibits in vivo tumor growth by a mechanism that is independent of significant gap junctional intercellular communication

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The role of connexin-mediated cell-cell communication in breast cancer metastasis

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Modulation of mouse neural crest cell motility by N-cadherin and connexin 43 gap junctions

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RhoA is required for monocyte tail retraction during transendothelial migration

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Breast cancer metastatic potential correlates with a breakdown in homospecific and heterospecific gap junctional intercellular communication

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Exogenous expression of N-cadherin in breast cancer cells induces cell migration, invasion, and metastasis

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N-cadherin promotes motility in human breast cancer cells regardless of their E-cadherin expression

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Genetic diseases and gene knockouts reveal diverse connexin functions.

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28 September 2017

Suppression of human prostate cancer cell growth by forced expression of connexin genes

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Frequent reduction of gap junctional intercellular communication and connexin43 expression in human and mouse lung carcinoma cells

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Independence of metastatic ability and extravasation: metastatic ras-transformed and control fibroblasts extravasate equally well

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28 September 2017

Connections with connexins: the molecular basis of direct intercellular signaling

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Intercellular communication and carcinogenesis

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Loss of epithelial differentiation and gain of invasiveness correlates with tyrosine phosphorylation of the E-cadherin/beta-catenin complex in cells transformed with a temperature-sensitive v-SRC gene

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Connexin40, a component of gap junctions in vascular endothelium, is restricted in its ability to interact with other connexins

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Connexin 43 and connexin 40 gap junctional proteins are present in arteriolar smooth muscle and endothelium in vivo

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12 December 2020

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Deficiency of connexin43 gap junctions is an independent marker for breast tumors

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12 December 2020

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Medicine. Tracing the steps of metastasis, cancer's menacing ballet

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Serum leptin, prolactin and vascular endothelial growth factor (VEGF) levels in patients with breast cancer

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12 December 2020

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Autocrine regulation of myocyte Cx43 expression by VEGF

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12 December 2020

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Rapid analysis of leukocyte-endothelial adhesion

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12 December 2020

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Decreased E-cadherin immunoreactivity correlates with poor survival in patients with bladder tumors

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12 December 2020

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Fate of melanoma cells entering the microcirculation: over 80% survive and extravasate

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12 December 2020

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Aberrant expression of gap junction proteins (connexins) is associated with tumor progression during multistage mouse skin carcinogenesis in vivo

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12 December 2020

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Integrin expression in breast cancer cytology: a novel predictor of axillary metastasis

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12 December 2020

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Porcine aortic endothelial gap junctions: identification and permeation by caged InsP3

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Identifiers

DOI

10.1186/BCR1042

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1396479

Dimensions Publication ID

1019065619

0 references

OpenCitations bibliographic resource ID

1396479

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1396479

PMC publication ID

1175070

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1396479

PubMed publication ID

15987459

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1396479

ResearchGate publication ID

7757403

0 references

 

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