How a 73-year-old heavy smoker’s ‘velvety’ palms turned out to be a sign of lung cancer



The unnamed woman, of São Paulo, Brazil, had ‘tripe palms’ – often the sign of an underlying cancer. Tests revealed the woman had adenocarcinoma and she had treatment.

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Authors: Patil T, Simons E, Mushtaq R, Pacheco JM, Doebele RC, Bowles DW
ROS1 gene fusions account for approximately 1-2% of all cases of non-small cell lung cancer (NSCLC). Similarly to anaplastic lymphoma kinase (ALK)-positive NSCLC, patients with ROS1+ NSCLC tend to have minimal smoking and be of the female sex. In most cases, adenocarcinoma is the dominant histology. The ROS1 gene has homology to ALK and this structural similarity formed the basis for utilizing ALK inhibitors for ROS1+ NSCLC. On the basis of impressive progression-free survival of 19.2 months from the PROFILE 1001 trial, crizotinib obt…

Source: Drugs of TodayCategory: Drugs & Pharmacology Tags: Drugs Today (Barc) Source Type: research

Lung cancer is one of the most common types of cancer, among which lung adenocarcinoma accounts for the largest proportion. Currently, accurate staging is a prerequisite for effective diagnosis and treatment o…

Source: BMC BioinformaticsCategory: Bioinformatics Authors: Tags: Research article Source Type: research

Previous genome-wide transcriptome profiling found circ_ZNF124 was highly expressed in lung adenocarcinoma, however, the role of circ_ZNF124 in non-small cell lung cancer (NSCLC) is still unknown. The purpose …

Source: Cancer Cell InternationalCategory: Cancer & Oncology Authors: Tags: Primary research Source Type: research

Hua Dong
Yu Yao

While methods for detecting SNVs and indels in circulating tumor DNA (ctDNA) with hybridization capture-based next-generation sequencing (NGS) have been available, copy number variations (CNVs) detection is more challenging. Here, we present a method enabling CNV detection from a 150-gene panel using a very low amount of ctDNA. First, a read depth-based CNV estimation method without a paired blood sample was developed and cfDNA sequencing data from healthy people were used to build a panel of normal (PoN) model. Then, in silico and in vitro simulations were performed to define the limit of detecti…

Source: GenesCategory: Genetics & Stem Cells Authors: Tags: Article Source Type: research

Lung cancer is the most common cancer (11.6 % of total cancers) and the leading cause of death from cancers worldwide (18.4 % of total cancer deaths) [1], with adenocarcinoma being the most common histological type of lung cancer [2,3]. A new classification of lung adenocarcinoma was established in 2011, dividing lung adenocarcinoma into atypical adenomatous hyperplasia (AAH), adenocarcinoma in situ (AIS), minimally invasive adenocarcinoma (MIA) and invasive adenocarcinoma (IAC) [4], consistent with the classification of lung adenocarcinoma published by WHO in 2015 [5].

Source: Lung CancerCategory: Cancer & Oncology Authors: Source Type: research

ConclusionSeveral radiomic features (including wavelet energies, information measures of correlation and maximum probability from co-occurrence matrix, busyness from neighborhood intensity-difference matrix, directionalities from Tamura ’s texture, and fractal dimension estimation) significantly associated with distant metastasis, nodal metastasis, and histology were discovered in this work, presenting great potential as imaging biomarkers for pathological diagnosis and target therapy decision.

AbstractBackground.Non‐small cell lung cancer (NSCLC) is one of the most common human malignancies and the leading cause of cancer‐related death. Over the past few decades, genomic alterations of cancer driver genes have been identified in NSCLC, and molecular testing and targeted therapies have become standard care for lung cancer patients. Here we studied the unique genomic profile of driver genes in Chinese patients with NSCLC by next‐generation sequencing (NGS) assay.Materials and Methods.A total of 1,200 Chinese patients with NSCLC were enrolled in this study. The median age was 60 years (range: 26–…

Source: The OncologistCategory: Cancer & Oncology Authors: Tags: Cancer Diagnostics and Molecular Pathology Source Type: research

Conclusion.As a noninvasive method, the CT‐based radiomics signature can be used to predict the EGFR mutation status of LADC appearing as a subsolid nodule.Implications for Practice.Lung adenocarcinoma (LADC) with epidermal growth factor receptor (EGFR) mutation is considered a subgroup of lung cancer that is sensitive to EGFR‐targeted tyrosine kinase inhibitors. However, some patients with inoperable subsolid LADC are unable to undergo tissue sampling by biopsy for molecular analysis in clinical practice. A computed tomography‐based radiomics signature may serve as a noninvasive biomarker to predict the EGFR mutatio…

Source: The OncologistCategory: Cancer & Oncology Authors: Tags: Lung Cancer, Precision Medicine Clinic: Molecular Tumor Board, Cancer Imaging, Cancer Diagnostics and Molecular Pathology Source Type: research

ConclusionOverexpression of miR ‐191‐5p is capable of blocking the migration and proliferation of lung cancer cells, and its mechanism may be through targetingSATB1 thus downregulating Wnt signaling.

Source: Molecular Genetics & Genomic MedicineCategory: Genetics & Stem Cells Authors: Tags: ORIGINAL ARTICLE Source Type: research

In conclusion, our findings indicate that IL-4/STAT6 signaling in CD11b+ cells promotes lung cancer progression by triggering an IL-4 positive feedback loop and increasing M2 myeloid cells. STAT6 may be a new therapeutic target for the prevention and treatment of lung cancer.


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