Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We discuss the influence of the microenvironment and driver mutations on TPCs formation and function, the existence of phenotypically distinct TPC clones within a tumor, the evolution of TPCs with disease progression, and their implications for therapy.
|
31801972 |
2020 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
We describe a case of papillary thyroid carcinoma with fibromatosis/fasciitis-like stroma (PTC-FLS) that contained the rare BRAF c.1799_1801delTGA (p.V600_K601delinsE) mutation, which has not previously been reported in this tumour, as well as the CTNNB1 c.133T>C (p.S45P) mutation.
|
31327063 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
CCDC6 was barely detected in 30% of the tumors that also carried BAP1 defects.
|
31447003 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Deficiency of the tumor suppressor CCDC6 determines PARP-inhibitor sensitivity.
|
30786932 |
2019 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
TERT promoter mutations correlated with older age (P < 0.0001), larger tumor size (P = 0.0002), oxyntic and aggressive PTC variants (P = 0.01), higher tumor stages (P < 0.0001), distant metastases (<0.0001) and disease outcome (P < 0.0001).
|
31042674 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
CCDC6, one of the players in DNA repair system acts as a tumor suppressor gene.
|
30909182 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
<b>Methods:</b> Here, we investigated the impact of PTC-209, a small-molecule Bmi-1 inhibitor, on human cancer cell viability alone and in combination with anticancer drugs, namely, cisplatin, oxaliplatin, 5-fluorouracil, camptothecin, and Frondoside-A and its impact on cellular migration and colony growth <i>in vitro</i> and on tumor growth <i>in ovo</i>.
|
31695609 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Incidence of bilateral tumors is high and increases with the number of tumor foci in multifocal PTC.
|
30851890 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Correction to: Application of Strict Criteria for Noninvasive Follicular Thyroid Neoplasm with Papillary-Like Nuclear Features and Encapsulated Follicular Variant Papillary Thyroid Carcinoma: a Retrospective Study of 50 Tumors Previously Diagnosed as Follicular Variant PTC.
|
29923169 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our analysis showed that tumor multifocality rather than size is the significant factor determining prognosis; hence, total thyroidectomy is indicated for an optimal assessment of true focality in micro-PTC.
|
28550398 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Several CCDC6 mutations and gene rearrangements have been described so far in different types of cancer and CCDC6 may represent a possible predictive biomarker of tumor resistance to the conventional anticancer treatments.
|
29044514 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
And Chromatin Immunoprecipitation assay confirms that the derepressed tumor suppressor genes belong to BMI-1 targets and the enrichment levels of H2AK119ub1 at their promoters is decreased upon PTC-209 treatment.
|
29886801 |
2018 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
- Proposed noninvasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTPs), formerly noninvasive encapsulated papillary carcinoma, follicular variant (PTC-FV), is an indolent tumor with follicular growth and frequent RAS mutations.
|
29582677 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In an aggressive uterine carcinosarcoma xenograft model, single-agent PTC-028 significantly delayed tumor growth and increased tumor doubling time compared with the standard carboplatin/paclitaxel therapy.
|
30026381 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
FNA = fine-needle aspiration; GEC = gene expression classifier; NIFTP = noninvasive follicular thyroid neoplasm with papillary-like nuclear features; PTC = papillary thyroid cancer; SFN = suspicious for follicular neoplasia.
|
30084677 |
2018 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Two coding fusions (CCDC6-RET and LMO7-BRAF) were found in one tumor sample each.
|
29768105 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Application of Strict Criteria for Noninvasive Follicular Thyroid Neoplasm with Papillary-Like Nuclear Features and Encapsulated Follicular Variant Papillary Thyroid Carcinoma: a Retrospective Study of 50 Tumors Previously Diagnosed as Follicular Variant PTC.
|
29368294 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
So, here, on the basis of our recent findings on the role of the tumor suppressor CCDC6 protein in lung tumorigenesis, we will also discuss novel therapeutic approaches we envision for lung cancer.
|
28653990 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The multifocality rate of PTC was 35.1% and mPTC were shown to have larger primary tumor diameter, higher rate of lymph node metastasis and less number of accompanying non-cancerous lesions than single PTC in one or both gender groups.
|
28315434 |
2017 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Using chemical genomics in conjunction with phosphoproteomic analyses in <i>RET</i>-rearranged cells, we identify the CCDC6-RET<sup>I788N</sup> mutation and drug-induced mitogen-activated protein kinase pathway reactivation as possible mechanisms by which tumors may escape the activity of RET inhibitors.
|
28615362 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our results show that PTC presented different patterns of PN immunoreaction, stromal PN being significantly associated with advanced tumor stage and extrathyroidal extension.
|
29435461 |
2017 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
In contrast, KIF5B-RET and CCDC6-RET fusion genes have been identified in 70% to 90% and 10% to 25% of tumors, respectively.
|
28082048 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Importantly, in vivo PTC-209 administration significantly reduced tumor growth in a HNSCC xenograft model probably by Bmi1 inhibition and impaired cell proliferation.
|
29200967 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
FAK inhibition, with PF-562,271 treatment, modestly reduced tumor volumes, while FAK depletion, through shRNA knockdown, significantly reduced tumor volumes in vivo A role for FAK expression in tumor establishment was demonstrated in a model of PTC, where FAK knockdown tumors did not develop.
|
27259715 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Targeting of BMI-1 with PTC-209 shows potent anti-myeloma activity and impairs the tumour microenvironment.
|
26935956 |
2016 |