Search Results - "Y CAJAL, Teresa Ramon"
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Risk of Cancer in Family Members of Patients with Lynch-Like Syndrome
Published in Cancers (09-08-2020)“…Lynch syndrome (LS) is a common cause of hereditary colorectal cancer (CRC). Some CRC patients develop mismatch repair deficiency without germline pathogenic…”
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Circulating microRNAs in Early Breast Cancer Patients and Its Association With Lymph Node Metastases
Published in Frontiers in oncology (26-08-2021)“…MicroRNAs have emerged as important regulators of the metastatic process. In addition, circulating miRNAs appear to be surprisingly stable in peripheral blood…”
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3
Prevalence of germline MUTYH mutations among Lynch-like syndrome patients
Published in European journal of cancer (1990) (01-09-2014)“…Abstract Background and aims Individuals with tumours showing mismatch repair (MMR) deficiency not linked to germline mutations or somatic methylation of MMR…”
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Implications of Bariatric Surgery in Patients with Familial Adenomatous Polyposis Requiring Proctocolectomy with Ileal Pouch Anal Anastomosis
Published in Obesity surgery (01-11-2020)Get full text
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BRCA1 loss activates cathepsin L-mediated degradation of 53BP1 in breast cancer cells
Published in The Journal of cell biology (21-01-2013)“…Loss of 53BP1 rescues BRCA1 deficiency and is associated with BRCA1-deficient and triple-negative breast cancers (TNBC) and with resistance to genotoxic drugs…”
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MicroRNA-1291 Is Associated With Locoregional Metastases in Patients With Early-Stage Breast Cancer
Published in Frontiers in genetics (02-12-2020)“…Evidence that microRNAs (miRNAs) regulate the various steps of metastasis is increasing. Several studies have looked at the miRNA expression profile in primary…”
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Comprehensive Constitutional Genetic and Epigenetic Characterization of Lynch-Like Individuals
Published in Cancers (05-07-2020)“…The causal mechanism for cancer predisposition in Lynch-like syndrome (LLS) remains unknown. Our aim was to elucidate the constitutional basis of mismatch…”
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8
Emotional functioning to screen for psychological distress in breast and colorectal cancer patients prior to adjuvant treatment initiation
Published in European journal of cancer care (01-05-2019)“…Introduction The objective was to analyze the usefulness of the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire…”
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9
Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic Characterization
Published in Cancers (05-11-2020)“…Hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC) is a very rare hereditary disorder characterized by cutaneous leiomyomas (CLMs), uterine…”
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10
Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer families
Published in Breast cancer research and treatment (01-02-2009)“…Recent reports have shown that mutations in the FANCJ/BRIP1 and FANCN/PALB2 Fanconi Anemia (FA) genes confer a moderate breast cancer risk. Discussion has been…”
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11
POT1 and Damage Response Malfunction Trigger Acquisition of Somatic Activating Mutations in the VEGF Pathway in Cardiac Angiosarcomas
Published in Journal of the American Heart Association (17-09-2019)“…Background Mutations in the gene explain abnormally long telomeres and multiple tumors including cardiac angiosarcomas (CAS). However, the link between long…”
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12
Mammographic density and breast cancer in women from high risk families
Published in Breast cancer research : BCR (11-07-2015)“…Mammographic density (MD) is one of the strongest determinants of sporadic breast cancer (BC). In this study, we compared MD in BRCA1/2 mutation carriers and…”
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13
Axitinib treatment in advanced RAI-resistant differentiated thyroid cancer (DTC) and refractory medullary thyroid cancer (MTC)
Published in European journal of endocrinology (01-10-2017)“…Background Axitinib, an antiangiogenic multikinase inhibitor (MKI), was evaluated in the compassionate use programme (CUP) in Spain (October 2012–November…”
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14
Effect of Mammography on Breast Cancer Risk in Women with Mutations in BRCA1 or BRCA2
Published in Cancer epidemiology, biomarkers & prevention (01-11-2006)“…Women who carry mutations in either the BRCA1 or BRCA2 genes are at risk for early-onset breast cancer and are recommended to begin screening mammography at…”
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15
Opinion about reproductive decision making among individuals undergoing BRCA1/2 genetic testing in a multicentre Spanish cohort
Published in Human reproduction (Oxford) (01-04-2009)“…BACKGROUND Mutations in breast cancer BRCA1/2 genes increase breast and ovarian cancer risk and are transmitted with an autosomal dominant pattern. Opinion…”
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Tumor analysis of MMR genes in Lynch‐like syndrome: Challenges associated with results interpretation
Published in Cancer medicine (Malden, MA) (01-04-2024)“…Background Up to 70% of suspected Lynch syndrome patients harboring MMR deficient tumors lack identifiable germline pathogenic variants in MMR genes, being…”
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The Average Cumulative Risks of Breast and Ovarian Cancer for Carriers of Mutations in BRCA1 and BRCA2 Attending Genetic Counseling Units in Spain
Published in Clinical cancer research (01-05-2008)“…Purpose: It is not clear that the published estimates of the breast and ovarian cancer penetrances of mutations in BRCA1 and BRCA2 can be used in genetic…”
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Chromosome 17 Centromere Duplication and Responsiveness to Anthracycline-Based Neoadjuvant Chemotherapy in Breast Cancer
Published in Neoplasia (New York, N.Y.) (01-10-2014)“…Abstract Human epidermal growth factor receptor 2 ( HER2 ) and topoisomerase II alpha ( TOP2A ) genes have been proposed as predictive biomarkers of…”
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19
Molecular detection of peripheral blood breast cancer mRNA transcripts as a surrogate biomarker for circulating tumor cells
Published in PloS one (18-09-2013)“…Circulating tumor cells (CTCs) are becoming a scientifically recognized indicator of primary tumors and/or metastasis. These cells can now be accurately…”
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SEOM–GEICAM–SOLTI clinical guidelines in advanced breast cancer (2022)
Published in Clinical & translational oncology (01-09-2023)“…Advanced breast cancer represents a challenge for patients and for physicians due its dynamic genomic changes yielding to a resistance to treatments. The main…”
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