Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
These skin fibroblasts, but not cells derived from unaffected individuals, showed lack of contact inhibition, decreased serum requirement for growth, elevated levels of plasminogen activator, and alterations in the intracellular distribution of actin cables; they did not, however, grow in the absence of anchorage, nor did they form palpable tumors in congenitally athymic BALB/c nu/nu mice, and they were normal with regard to cholesterol feedback regulation.
|
922693 |
1977 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
These findings imply that the primary transfectant strains develop subpopulations of cells that are selected to form tumors because of their elevated rate of exogenous mutant beta-actin synthesis.
|
3614199 |
1987 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
About 47% and 16% of these tumor samples also showed increased levels of ODC (mean 3.1-fold) and beta-actin (mean 1.6-fold) RNA, respectively.
|
1693276 |
1990 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
An antibody directed at the alfa-smooth muscle isoform of actin did not produce any positive staining in any of the tumors.
|
2282206 |
1990 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunostaining revealed that the tumors were positive for S-100 protein and vimentin and negative for glial fibrillary acidic protein, actin, and keratin.
|
2305928 |
1990 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The tumor promoter (TPA) does not modify the pattern of expression of the myf factors while it induces the accumulation of muscle-specific transcripts, such as alpha-actin and fast myosin light chain 1, and their corresponding proteins.
|
8395398 |
1993 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Different patterns for each marker suggested a developmental sequence of bladder cancer oncogenesis; G-actin was altered in 58% of distant biopsies (vs. 0/6 normals, P < 0.001), ploidy and cytology were altered in < 20% of distant fields and approximately 80% of tumors, and the other markers were intermediate.
|
8367495 |
1993 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These findings suggest that the increased actin organization, which appeared not to cause tumorigenic suppression in the microcell hybrids, is associated with complementation of tumor suppressor genes and senescence by multiple mechanisms.
|
8031469 |
1994 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
With the specific probes, all RMSs expressed alpha-CARD actin mRNA, four neoplasms expressed also alpha-smooth muscle actin mRNA, whereas the probe for alpha-SK actin mRNA never produced a signal except in one case, in which the tumor masses were intermingled with non-neoplastic preexistent striated muscle fibers.
|
8160781 |
1994 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Their expression in cultured pancreas cancer cells, normal pancreas tissue, and normal exocrine pancreas cultures was examined by Northern blotting. cDNA clones can be grouped into two broad categories: (1) those corresponding to genes expressed at high levels both in tumor cell lines and in primary cultures of normal pancreas, but not in normal tissue (i.e. thymosin beta4(3), cytokeratin 18, beta-actin, pyruvate kinase and mitochondrial genes); and (2) those corresponding to genes expressed at high levels in pancreas cancer cultures but not in normal pancreas tissue or cultured cells (i.e. tissue-type plasminogen activator and cathepsin H).
|
8641471 |
1996 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Variable reactions with keratins, alpha-smooth muscle actin, and epithelial membrane antigen (EMA) were found, as these markers were present in different cellular components of the tumors.
|
8989931 |
1996 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The first step of invasion and metastasis is the detachment of cancer cells in the primary tumor, which is mainly controlled by the function in the adherens junction, consisting of E-cadherin associated proteins (E-cadherin, alpha- and beta-catenins, vinculin, alpha-actinin, and actin).
|
8639463 |
1996 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Glial fibrillary acidic protein was positive in 8 cases (53%), and muscle-specific actin and smooth-muscle actin were positive in only 3 cases (20%); they were all cases of BME.Desmin was negative in all tumors.
|
8734420 |
1996 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
beta-Catenin is essential for the function of cadherins, a family of Ca2+-dependent cell-cell adhesion molecules, by linking them to (alpha)-catenin and the actin cytoskeleton. beta-Catenin also binds to adenomatous polyposis coli (APC) protein, a cytosolic protein that is the product of a tumor suppressor gene mutated in colorectal adenomas.
|
9024698 |
1997 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In addition, antibodies to alpha-smooth muscle actin strongly characterized the small basaloid cells of both types of neoplasm.
|
9129700 |
1997 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The primary tumor was clearly positive for á-smooth muscle type actin and desmin in moderately differentiated areas and indicated a loss of myogenic differentiation in other regions and therefore was classified as a poorly differentiated LMS.
|
9664117 |
1998 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tumor cells were usually reactive with antibodies to keratin (67 of 78 cases, 86%), epithelial membrane antigen (50 of 54, 93%), vimentin (64 of 66, 97%), desmin (70 of 78, 90%), neuron-specific enolase (60 of 74, 81%), and the EWS-WT1 chimeric protein (25 of 27, 93%); typically nonreactive for muscle common actin (one of 58, 2%), myogenin (zero of eight, 0%), and chromogranin (one of 46, 2%); and variably reactive for MIC2 (nine of 47, 20%) and p53 (five of 17 with > 20% tumor cells reactive).
|
9738572 |
1998 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Tumor specimens from all 14 patients in the good-prognosis group contained more than 10(3) IFN gamma mRNA copies per 5 x 10(5) beta actin mRNA copies, whereas tumor specimens from only six of the 13 patients in the poor-prognosis group contained this level of IFN gamma mRNA (two-sided P = .006).
|
9486814 |
1998 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
While B2M and ACTB exhibited comparable levels of expression within different grades of astrocytomas and meningiomas, GAPD showed an inverse pattern in these tumors.
|
10378372 |
1999 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Gelsolin, a regulator of the actin cytoskeleton, has been shown previously to act as a tumor suppressor in vitro and in vivo when introduced into certain cancer cell lines.
|
10505859 |
1999 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Mammalian severin (M-severin) isolated from LL/2-derived Lewis lung carcinoma tumors severed F-actin in a calcium-dependent manner, mimicking the function of Dictyostelium severin.
|
10537319 |
1999 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The reverse transcription-polymerase chain reaction technique was applied, and with beta-actin as internal standard, TGF-alpha and EGFR mRNA in laryngeal carcinomas, macroscopically normal laryngeal mucosas adjacent to the tumor and in vocal cord polyps were quantitatively examined.
|
11721445 |
1999 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Most tumors (19 of 25) were positive for CD117 (KIT) and for CD34 (16 of 27); six tumors coexpressed alpha-smooth muscle actin and CD117; none showed desmin or S-100 protein.
|
11023095 |
2000 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The expression of DTD and P450R in patient tumors (n = 29), as ratios to beta-actin levels, varied from 0 to 90% and 0 to 29%, respectively.
|
11350900 |
2001 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The comparison of the gene expression profiles between two subpopulations of melanoma cells (1C8 and T1C3) derived from the tumor of one patient by cDNA array revealed differences in GAPDH and beta-actin gene levels.
|
11476540 |
2001 |