Publications by authors named "B Bonsang"

Recurrent oncogenic drivers have been identified in a variety of sweat gland tumors. Recently, integration of human papillomavirus type 42 (HPV42) has been reported in digital papillary adenocarcinoma (DPA). The main objectives of the present study were (i) to provide an overview of the prevalence of previously identified oncogenic drivers in acral sweat gland tumors and (ii) to genetically characterize tumors in which no recurrent genetic alteration has been identified yet.

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Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder. The role of angiogenesis and VEGF pathway in the pathogenesis of neurofibromas and malignant peripheral nerve sheath tumors (MPNSTs) remains poorly understood. We assessed the expression of VEGF and VEGFR family members in cohorts of plexiform neurofibromas (pNF), MPNSTs and MPNST cell lines at transcript [pNF, n = 49; MPNST, n = 34] and protein levels [pNF, n = 21; MPNST, n = 9].

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Levels and sources of non-Methane Hydrocarbons (NMHCs) were investigated at the urban background Thissio station, close to the historical center of Athens (Greece) from March 2016 to February 2017 (12 months), by means of an automated GC-FID. Alkanes dominated over aromatics and alkenes, with hourly mean levels ranging from detection limit up to 60 μg m for i-pentane and 90 μg m for toluene. Higher levels were recorded in the cold period relative to the warmer one.

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Article Synopsis
  • Diffuse large B-cell lymphoma (DLBCL) is the most common type of lymphoid cancer in adults, and the role of the alternative NF-κB activation pathway, which involves the RelB subunit, in its development has not been well understood.
  • * Recent findings show that RelB is frequently activated in DLBCL patients across different subtypes, identifying a new patient group with unique genetic and expression features.
  • * This RelB-positive subgroup has a poor response to standard immunochemotherapy and demonstrates resistance to treatments like doxorubicin, highlighting the need for improved prognostic tools and targeted therapies for this DLBCL subset.
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