Osteosarcoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Our data indicated that miR-630 targets PSMC2 in OS and inhibited OS cell proliferation, which may offer a new mechanism underlying the development and progression of OS.
|
30915734 |
2019 |
Osteosarcoma of bone
|
0.020 |
Biomarker
|
disease |
BEFREE |
Our data indicated that miR-630 targets PSMC2 in OS and inhibited OS cell proliferation, which may offer a new mechanism underlying the development and progression of OS.
|
30915734 |
2019 |
Carcinogenesis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Proteasome 26S subunit ATPase 2 (<i>PSMC2</i>), a recently discovered gene, has been implicated in certain human carcinogenesis.
|
31598166 |
2019 |
Childhood Osteosarcoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Our data indicated that miR-630 targets PSMC2 in OS and inhibited OS cell proliferation, which may offer a new mechanism underlying the development and progression of OS.
|
30915734 |
2019 |
Osteosarcoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Silencing of PSMC2 was able to inhibit osteosarcoma cell motility, invasion as well as tumorigenicity in nude mice.
|
27888613 |
2017 |
Osteosarcoma of bone
|
0.020 |
Biomarker
|
disease |
BEFREE |
Silencing of PSMC2 was able to inhibit osteosarcoma cell motility, invasion as well as tumorigenicity in nude mice.
|
27888613 |
2017 |
Carcinogenesis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Proteasome 26S subunit ATPase 2 (PSMC2) is a recently identified gene potentially associated with certain human carcinogenesis.
|
27888613 |
2017 |
Childhood Osteosarcoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Silencing of PSMC2 was able to inhibit osteosarcoma cell motility, invasion as well as tumorigenicity in nude mice.
|
27888613 |
2017 |
Malignant Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
The expression levels of PSMC2 in cancer tissue were dramatically upregulated compared with adjacent normal tissues.
|
31715603 |
2019 |
Colorectal Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The results showed that, among the 96 CRC patients, the expression of PSMC2 was a positive correlation with the clinicopathological features of the patients with CRC.
|
31715603 |
2019 |
Primary malignant neoplasm
|
0.010 |
AlteredExpression
|
group |
BEFREE |
The expression levels of PSMC2 in cancer tissue were dramatically upregulated compared with adjacent normal tissues.
|
31715603 |
2019 |
Malignant neoplasm of colon and/or rectum
|
0.010 |
Biomarker
|
disease |
BEFREE |
Silencing of Proteasome 26S Subunit ATPase 2 Regulates Colorectal Cancer Cell Proliferation, Apoptosis, and Migration.
|
31715603 |
2019 |
Tumor Cell Invasion
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Current study was focused on elucidating the significance of PSMC2 on malignant behaviors in osteosarcoma including proliferation, apoptosis, colony formation, migration as well as invasion.
|
27888613 |
2017 |
Alveolar Soft Part Sarcoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
As a proof of principle, we describe two novel synthetic lethal interactions in human cells discovered by this approach, one between the tumor suppressor gene SMARCB1 and PSMA4, and another between alveolar soft-part sarcoma-associated ASPSCR1 and PSMC2.
|
23980094 |
2013 |
Adult Alveolar Soft Part Sarcoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
As a proof of principle, we describe two novel synthetic lethal interactions in human cells discovered by this approach, one between the tumor suppressor gene SMARCB1 and PSMA4, and another between alveolar soft-part sarcoma-associated ASPSCR1 and PSMC2.
|
23980094 |
2013 |
Childhood Alveolar Soft Part Sarcoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
As a proof of principle, we describe two novel synthetic lethal interactions in human cells discovered by this approach, one between the tumor suppressor gene SMARCB1 and PSMA4, and another between alveolar soft-part sarcoma-associated ASPSCR1 and PSMC2.
|
23980094 |
2013 |