Colorectal Carcinoma
|
0.320 |
AlteredExpression
|
disease |
BEFREE |
High levels of CENPH expression gradually decreased according to CRC tumor stages.
|
28819418 |
2017 |
Colorectal Carcinoma
|
0.320 |
AlteredExpression
|
disease |
BEFREE |
These results suggest that the aberrant expression and localization of a kinetochore protein CENP-H plays an important role in the aneuploidy frequently observed in colorectal cancers.
|
15930286 |
2005 |
Colorectal Carcinoma
|
0.320 |
GeneticVariation
|
disease |
UNIPROT |
|
|
|
Carcinogenesis
|
0.040 |
AlteredExpression
|
phenotype |
BEFREE |
<b>Background:</b> Centromere protein H (CENPH) is known as a fundamental component of the active centromere complex, and its overexpression is correlated with poor prognosis in various solid tumors. mTOR inhibitor rapamycin has been shown to possess antitumor activity, as well as prevent intestinal tumorigenesis.
|
28819418 |
2017 |
Carcinogenesis
|
0.040 |
Biomarker
|
phenotype |
BEFREE |
Centromere protein H (CENPH), one of the essential component of active kinetochore, plays an important role in carcinogenesis of many cancer types.
|
26248586 |
2015 |
Carcinogenesis
|
0.040 |
Biomarker
|
phenotype |
BEFREE |
Centromere protein H (CENP-H) is one of the essential components of the human active kinetochore which close links with carcinogenesis.
|
22999412 |
2013 |
Carcinogenesis
|
0.040 |
Biomarker
|
phenotype |
BEFREE |
Recently, CENP-H was identified to be associated with tumorigenesis.
|
19500341 |
2009 |
Malignant Neoplasms
|
0.030 |
AlteredExpression
|
group |
BEFREE |
Centromere protein H (CENP-H) has been shown to be significantly upregulated in many types of cancers and is associated with disrupted cell cycle regulation, cell proliferation and genetic instability.
|
23970101 |
2013 |
Malignant Neoplasms
|
0.030 |
Biomarker
|
group |
BEFREE |
Increased CENP-H or Ki67 were associated with short relapse-free survival (P<0.001 or P=0.009, respectively) and were independent predictors of relapse-free survival (P=0.001 and P=0.018, respectively). siRNA knockdown of CENP-H mRNA inhibited cell proliferation and promoted cancer cell apoptosis in vitro.
|
22631655 |
2012 |
Malignant Neoplasms
|
0.030 |
GeneticVariation
|
group |
BEFREE |
We found somatic frameshit mutations of the KNTC1 (6.7% GC, 12.1% CRC), ZC3H13 (3.3% GC, 15.2% CRC), CENPH (6.7% GC), TOPBP1 (3.0% CRC), NDCO80 (3.0% CRC), RIF1 (6.7% GC), and NBS1 (3.3% GC, 3.0% CRC) genes in the cancers with MSI-H. Mutations were detected in MSI-H, but not in MSI-L or MSS samples.
|
21388066 |
2011 |
Malignant neoplasm of colon and/or rectum
|
0.020 |
Biomarker
|
disease |
BEFREE |
CENPH Inhibits Rapamycin Sensitivity by Regulating GOLPH3-dependent mTOR Signaling Pathway in Colorectal Cancer.
|
28819418 |
2017 |
Malignant neoplasm of stomach
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Furthermore, total mRNA and protein expression of CENP-H in GC tissue and cell lines were noticeably increased.
|
22999412 |
2013 |
Stomach Carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Furthermore, total mRNA and protein expression of CENP-H in GC tissue and cell lines were noticeably increased.
|
22999412 |
2013 |
Malignant neoplasm of stomach
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
We found somatic frameshit mutations of the KNTC1 (6.7% GC, 12.1% CRC), ZC3H13 (3.3% GC, 15.2% CRC), CENPH (6.7% GC), TOPBP1 (3.0% CRC), NDCO80 (3.0% CRC), RIF1 (6.7% GC), and NBS1 (3.3% GC, 3.0% CRC) genes in the cancers with MSI-H. Mutations were detected in MSI-H, but not in MSI-L or MSS samples.
|
21388066 |
2011 |
Stomach Carcinoma
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
We found somatic frameshit mutations of the KNTC1 (6.7% GC, 12.1% CRC), ZC3H13 (3.3% GC, 15.2% CRC), CENPH (6.7% GC), TOPBP1 (3.0% CRC), NDCO80 (3.0% CRC), RIF1 (6.7% GC), and NBS1 (3.3% GC, 3.0% CRC) genes in the cancers with MSI-H. Mutations were detected in MSI-H, but not in MSI-L or MSS samples.
|
21388066 |
2011 |
Malignant neoplasm of colon and/or rectum
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Centromere protein H is up-regulated in primary human colorectal cancer and its overexpression induces aneuploidy.
|
15930286 |
2005 |
Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
High levels of CENPH expression gradually decreased according to CRC tumor stages.
|
28819418 |
2017 |
Solid Neoplasm
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
<b>Background:</b> Centromere protein H (CENPH) is known as a fundamental component of the active centromere complex, and its overexpression is correlated with poor prognosis in various solid tumors. mTOR inhibitor rapamycin has been shown to possess antitumor activity, as well as prevent intestinal tumorigenesis.
|
28819418 |
2017 |
Renal Cell Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
In conclusion, our data suggest that CENPH is a novel molecule involved in RCC progression, which provides a potential biomarker and therapeutic target.
|
26248586 |
2015 |
Neoplasm Metastasis
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
Further statistical analysis suggested the upregulation of CENPH was positively correlated with the Fuhrman grade (P = 0.001), distant metastasis (P = 0.024) and clinical stage (P = 0.014).
|
26248586 |
2015 |
Conventional (Clear Cell) Renal Cell Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
In conclusion, our data suggest that CENPH is a novel molecule involved in RCC progression, which provides a potential biomarker and therapeutic target.
|
26248586 |
2015 |
Liver carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
CENP-H was overexpressed in HCC, and its level of upregulation was an independent prognostic indicator, suggesting that CENP-H may be an effective therapeutic strategy for the treatment of HCC.
|
23970101 |
2013 |
Hypopharyngeal Cancer
|
0.010 |
Biomarker
|
disease |
BEFREE |
Role of centromere protein H and Ki67 in relapse-free survival of patients after primary surgery for hypopharyngeal cancer.
|
22631655 |
2012 |
Squamous cell carcinoma of the hypopharynx
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Upregulated CENP-H and Ki67 levels are significantly associated with short relapse-free survival in HSCC.
|
22631655 |
2012 |
Primary malignant neoplasm
|
0.010 |
Biomarker
|
group |
BEFREE |
Increased CENP-H or Ki67 were associated with short relapse-free survival (P<0.001 or P=0.009, respectively) and were independent predictors of relapse-free survival (P=0.001 and P=0.018, respectively). siRNA knockdown of CENP-H mRNA inhibited cell proliferation and promoted cancer cell apoptosis in vitro.
|
22631655 |
2012 |