Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Only 2 cases showed a focal (10% of the tumor) membranous staining of Cx43.
|
31809272 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Connexin 43 (Cx43) protein and its cell-communication channels have been assigned tumor suppressor functions while the anti-apoptotic Bcl-2 (B-cell lymphoma-2) protein has been associated with negative prognostic significance in cancer.
|
31766723 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Because Cx43 can either act as a tumor suppressor or oncogene, biomarker analysis and a better understanding of how Cx43 contextually mediates cancer phenotypes will be required to develop clinically viable Cx43-based therapies.
|
30472182 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, this article summarize the prognostic value of Cx43 and offer a clinical evidence for the notion that Cx43 is generally a tumor suppressor and beneficial for the patients' survival time.
|
31781504 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Univariate and multivariate logistic analyses showed that irregular tumor shape (P = 0.010) and low Cx43 expression (P = 0.010) were independent predictors of the presence of MP, and the predicted probability was calculated by the following formula: P = 1/[1+exp.{1.218-(3.202×Shape)+(3.814×Cx43)}].
|
30822595 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, it was shown that by using CLSM and super-resolution SMLM, treatment effects on the spatial and thus functional arrangements of Cx43 became detectable for investigations of tumor response mechanisms.
|
30836676 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Cx43 expression was independent of tumor size, grade, stage and ER-status in predicting poor survival on multivariate analysis (p = 0.004).
|
30474779 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Connexin 43 (Cx43) is involved in enhancing chemosensitivity that was suppressed in a tumor microenvironment.
|
31217730 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The focal adhesion kinase (FAK) and gap junction protein connexin 43 (Cx43) are involved in the occurrence and progression of tumors.
|
31773683 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, we found Cx43, Cx26 and Cx30 proteins upregulated in the melanoma adjacent epidermis, and Cx43 in the tumor flanking vessels.
|
30717194 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Collectively, Cx43 over-expression induced an epithelial-like phenotype in MDA-MB-231 cells and suppressed tumor growth and metastasis to secondary organs in vivo.
|
30939738 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Additionally, the presence of Cx43-mediated GJIC could decrease the mean RTV and tumor weights of xenografts after Photofrin-PDT.
|
30745846 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We discuss how these abnormalities will support tumor survival via the actions of gap junctions (GJs) and hemichannels (HCs) which are composed of hexamer of connexin43 (Cx43) protein.
|
29641478 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Targeting these domains of Cx43, which is expressed in distinct patterns in the heterogeneous glioma cell population, can inhibit tumor cell invasion and new tumor formation.
|
29106645 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
A better understanding of Cx43 regulation in a subtype-dependent manner is needed to clarify the context in which Cx43 is associated with tumor suppression or cancer progression.
|
29495625 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
As observed in several other types of solid tumours, Cxs and especially Cx43 exhibit an ambivalent role with a tumour suppressor effect in the early stages and, conversely, a rather pro-tumoural profile for most of invasion and dissemination steps to secondary sites.
|
28693897 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
This review summarizes recent advances in understanding the roles of Cx43 in malignant glioma, with a special focus on tumor microenvironment, TMZ resistance, and therapeutic opportunity offered by Cx43 peptidomimetics.
|
29803991 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Connexin 43 (Cx43; also known as GJA1) is the most abundantly expressed gap junction channel protein in humans and acts as a tumor suppressor in multiple tissue types.
|
28733455 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In conclusion, dioscin targets Cx43 to suppress the tumor cell malignancy and activate macrophage sensitivity, thereby targeting melanoma microenvironment.
|
28677156 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Connexin-43 enhances tumor suppressing activity of artesunate via gap junction-dependent as well as independent pathways in human breast cancer cells.
|
28790385 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Available evidence reveals Cx43 as a tumor‑inhibiting factor that suppresses glioma growth and proliferation.
|
28983585 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Cx43 protein expression in hepatic and PM was significantly higher than that in the primary tumor, while no significant difference was showed in messenger RNA (mRNA) expression.
|
26879016 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Indeed, restoring Cx43 to glioma cells reduces their rate of proliferation and their tumorigenicity but this tumor suppressor effect could be counterbalanced by its effects on invasiveness, adhesion and migration.
|
25711938 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, both Cx43 osteocyte-specific knockout mice and osteocyte-specific Δ130-136 transgenic mice with impaired Cx43 gap junctions and hemichannels showed significantly increased tumor growth and attenuated the inhibitory effect of ZOL.
|
27041582 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Significantly less Cx43 was detected in α-smooth muscle actin positive than α-smooth muscle actin negative stromal cells and in osteoclast-rich tumor nests than in the adjacent reactive stroma.
|
25933380 |
2015 |