Neoplasms
|
0.050 |
AlteredExpression
|
group |
BEFREE |
RINF expression was significantly higher in all tumor forms (primary breast, and thyroid cancers and metastatic melanomas) as compared with normal control tissues (P < 0.001 for each comparison).
|
21325450 |
2011 |
Neoplasms
|
0.050 |
AlteredExpression
|
group |
BEFREE |
Finally, CXXC5 knockdown in human AML cell lines caused significantly increased expression of the potential tumor suppressor gene TSC22 and genes encoding the growth factor receptor KIT, the cytokine Angiopoietin 1 and the selenium-containing glycoprotein Selenoprotein P. Thus, high CXXC5 expression seems to affect several steps in human leukemogenesis, including intracellular events as well as extracellular communication.
|
25605239 |
2015 |
Leukemia, Myelocytic, Acute
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
Inactivation of CXXC5 is associated with different leukemic pathways and defines an AML subgroup with better outcome.
|
25805812 |
2015 |
Malignant neoplasm of breast
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
Notably, high levels of RINF was strongly associated with TP53 wild-type status (P = 0.002) possibly indicating that high levels of RINF could substitute for TP53 mutations as an oncogenic mechanism during the malignant development of some cases of breast cancer.
|
21325450 |
2011 |
Leukemogenesis
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
Finally, CXXC5 knockdown in human AML cell lines caused significantly increased expression of the potential tumor suppressor gene TSC22 and genes encoding the growth factor receptor KIT, the cytokine Angiopoietin 1 and the selenium-containing glycoprotein Selenoprotein P. Thus, high CXXC5 expression seems to affect several steps in human leukemogenesis, including intracellular events as well as extracellular communication.
|
25605239 |
2015 |
Leukemogenesis
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
In gene-expression profiling, lower CXXC5 expression was associated with upregulation of cell-cycling genes and co-downregulation of genes implicated in leukemogenesis (WT1, GATA2, MLL, DNMT3B, RUNX1).
|
25805812 |
2015 |
Breast Carcinoma
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
Notably, high levels of RINF was strongly associated with TP53 wild-type status (P = 0.002) possibly indicating that high levels of RINF could substitute for TP53 mutations as an oncogenic mechanism during the malignant development of some cases of breast cancer.
|
21325450 |
2011 |
Papillary thyroid carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
CXXC5 is a gene encoding a retinoid-inducible nuclear factor, whose overexpression in breast tumours, metastatic malignant melanomas and papillary thyroid carcinoma has been recently reported.
|
29027288 |
2017 |
Papillary thyroid carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
RINF messenger RNA expression was examined in biopsies from locally advanced breast tumors, metastatic malignant melanomas, and papillary thyroid carcinomas and compared with their paired or nonpaired normal reference samples.
|
21325450 |
2011 |
Mammary Neoplasms
|
0.020 |
AlteredExpression
|
group |
BEFREE |
CXXC5 is a gene encoding a retinoid-inducible nuclear factor, whose overexpression in breast tumours, metastatic malignant melanomas and papillary thyroid carcinoma has been recently reported.
|
29027288 |
2017 |
Mammary Neoplasms
|
0.020 |
AlteredExpression
|
group |
BEFREE |
Our data indicate that (i) RINF overexpression is associated with the malignant phenotype in solid tumors and (ii) RINF overexpression represents an independent molecular marker for poor prognosis in breast tumors.
|
21325450 |
2011 |
Liver carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Moreover, knockdown of PSMB2 or CXXC5 suppresses HCC cell proliferation and invasion.
|
29780166 |
2018 |
Malignant neoplasm of thyroid
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
RINF expression was significantly higher in all tumor forms (primary breast, and thyroid cancers and metastatic melanomas) as compared with normal control tissues (P < 0.001 for each comparison).
|
21325450 |
2011 |
melanoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
RINF expression was significantly higher in all tumor forms (primary breast, and thyroid cancers and metastatic melanomas) as compared with normal control tissues (P < 0.001 for each comparison).
|
21325450 |
2011 |
Tumor Progression
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
CXXC5 expression in prostate cancer: implications for cancer progression.
|
29027288 |
2017 |
Malignant neoplasm of prostate
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
CXXC5 mRNA and protein expressions were significantly higher in prostate cancer, high-grade prostatic intra-epithelial neoplasia, and proliferative inflammatory atrophy, compared to benign prostate tissue.
|
29027288 |
2017 |
Thyroid carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
RINF expression was significantly higher in all tumor forms (primary breast, and thyroid cancers and metastatic melanomas) as compared with normal control tissues (P < 0.001 for each comparison).
|
21325450 |
2011 |
Prostate carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
CXXC5 mRNA and protein expressions were significantly higher in prostate cancer, high-grade prostatic intra-epithelial neoplasia, and proliferative inflammatory atrophy, compared to benign prostate tissue.
|
29027288 |
2017 |
Oestrogen receptor positive breast cancer
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
These results suggest that overexpression of CXXC5 is a strongly poor prognostic factor in ER+ breast cancer.
|
29928427 |
2018 |
Proliferative Inflammatory Atrophy
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
CXXC5 mRNA and protein expressions were significantly higher in prostate cancer, high-grade prostatic intra-epithelial neoplasia, and proliferative inflammatory atrophy, compared to benign prostate tissue.
|
29027288 |
2017 |
Locally advanced breast cancer
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Further, the prognostic role of RINF expression was evaluated in locally advanced breast cancer.
|
21325450 |
2011 |
Diminished ovarian reserve
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Forty-eight transcripts were differentially expressed, including CXXC finger protein 5 (CXXC5), forkhead box C1 (FOXC1) (down-regulated in DOR) as well as connective tissue growth factor (CTGF), follistatin-like 3 (FSTL3), prostaglandin-endoperoxide synthase 2 (PTGS2) and suppressor of cytokine signaling 2 (SOCS2) (up-regulated in DOR).
|
22246450 |
2012 |
estrogen receptor-negative breast cancer
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
These results suggest that overexpression of CXXC5 is a strongly poor prognostic factor in ER+ breast cancer.
|
29928427 |
2018 |
Neoplasms
|
0.050 |
Biomarker
|
group |
BEFREE |
Interestingly, RINF localizes to 5q31.3, a small region often deleted in myeloid leukemia (acute myeloid leukemia [AML]/myelodysplasia [MDS]) and suspected to harbor one or several tumor suppressor gene.
|
19182210 |
2009 |
Neoplasms
|
0.050 |
Biomarker
|
group |
BEFREE |
These observations together suggest that CXXC5 may act as a tumor suppressor by promoting TGF-β signaling via a positive feedback loop, and reveal a strategy for HCC to bypass TGF-β-mediated cytostasis by disrupting the positive feedback regulation.
|
29036306 |
2018 |