Formation of chloramphenicol resistant (CMr) spontaneous and nitroso-ethyl-urea-induced mutants of S.erythraea, an organism producing erythromycin, was studied. The mutants differed by the level of the chloramphenicol resistance (10 to 40 micrograms/ml). Part of the chloramphenicol resistance mutations had a pleiotropic pattern. 63.8 per cent of the CMr mutants was characterized by the growth thermosensitivity and 18.9 per cent was characterized by the absence of the melanin production property. The antibiotic potency of 56 per cent of the CMr mutants was higher than that of the initial strain. In some of the CMr mutants the property of resistance to other antibiotics was changed. A higher resistance of some mutants to chloramphenicol correlated with their increased lincomycin resistance. It was shown that chloramphenicol induced resistance to kanamycin in S.erythraea 5. Such a property for the resistance induction was preserved in the spontaneous low CMr mutants while the high CMr mutants isolated after the culture exposure to the mutagen lacked it. The CMr S.erythraea phenotype was genetically instable. Two different amplifying DNA sequences (18 and 70-78 kb in size) were detected in the CMr mutant genome. The chloramphenicol resistance mutation was localized in the S.erythraea chromosome region restricted by markers ura1 and met1.
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Ann Hematol
November 2024
National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, the First Affiliated Hospital of Soochow University, Soochow University, Suzhou, People's Republic of China.
Olverembatinib is a novel orally administered third-generation tyrosine kinase inhibitor (TKI) with definitive responses in T315I-mutant chronic myeloid leukemia (CML) patients. However, its value in newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) remained unclarified. In this multiple-center study, 20 patients with de novo Ph + ALL were treated with olverembatinib-based regimens as frontline therapy.
View Article and Find Full Text PDFJ Thromb Haemost
April 2024
Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA. Electronic address:
Clin Cancer Res
September 2023
Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, New York.
Purpose: Small-cell lung cancer (SCLC) is a high-grade neuroendocrine tumor with dismal prognosis and limited treatment options. Lurbinectedin, conditionally approved as a second-line treatment for metastatic SCLC, drives clinical responses in about 35% of patients, and the overall survival (OS) of those who benefit from it remains very low (∼9.3 months).
View Article and Find Full Text PDFMol Genet Genomic Med
September 2023
Heart Center, The First Hospital of Lanzhou University, Lanzhou, Gansu, China.
Background: Danon disease is characterized by the failure of lysosomal biogenesis, maturation, and function due to a deficiency of lysosomal membrane structural protein (LAMP2).
Methods: The current report describes a female patient with a sudden syncope and hypertrophic cardiomyopathy phenotype. We identified the pathogenic mutations in patients by whole-exon sequencing, followed by a series of molecular biology and genetic approaches to identify and functional analysis of the mutations.
ESMO Open
April 2023
Yale Cancer Center, New Haven, USA.
Background: Acquired resistance limits long-term epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) efficacy in patients with EGFR mutation-positive non-small-cell lung cancer (NSCLC) in whom anti-programmed death-ligand 1 (PD-L1) efficacy is also limited. We hypothesized that combining atezolizumab with erlotinib could enhance antitumor immunity and extend efficacy in these patients.
Patients And Methods: This open-label phase Ib trial was conducted in adults aged ≥18 years who had advanced, unresectable NSCLC.
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