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1.
BMJ Case Rep ; 20182018 May 12.
Article in English | MEDLINE | ID: mdl-29754130

ABSTRACT

The incidence of urothelial carcinoma (UC; formerly transitional cell carcinoma) is higher among renal transplant recipients compared with the general population. Upper urinary tract UC (UUT-UC) of allograft urothelium is a rare event with approximately 40 cases reported in the literature. Herein, we describe the clinical presentation and management of UUT-UC in a transplant ureter 10 years after deceased donor kidney transplantation.


Subject(s)
Carcinoma, Transitional Cell/pathology , Cystectomy , Kidney Failure, Chronic/surgery , Kidney Transplantation , Nephrectomy , Ureter/pathology , Urologic Neoplasms/pathology , Aged , Carcinoma, Transitional Cell/diagnostic imaging , Carcinoma, Transitional Cell/surgery , Humans , Kidney/pathology , Male , Time Factors , Transplantation, Homologous , Treatment Outcome , Ureter/diagnostic imaging , Ureter/surgery , Urologic Neoplasms/diagnostic imaging , Urologic Neoplasms/surgery
2.
Curr Opin Pulm Med ; 19(1): 66-72, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23095468

ABSTRACT

PURPOSE OF REVIEW: Asthma is a global disease affecting millions of people. Current treatments are largely symptomatic and, although often effective, can be associated with various side effects. microRNAs (miRNAs/miRs) are regulatory RNAs that affect protein synthesis. They represent new therapeutic targets, and medicines that target specific miRNAs may have potential in the treatment of asthma. RECENT FINDINGS: There have been a number of studies in the field of miRNA that implicate specific miRNAs in the pathophysiology of asthma. For example, studies using mouse models have identified miRNAs that are altered in response to allergen challenge. Certain miRNAs that are involved in the regulation of interleukin-13 and the TH2 response, key components of the asthmatic response, have been shown to be amenable to modulation by premiRs and antimiRs. Other studies have identified miRNAs that are implicated in bronchial smooth muscle hyperresponsiveness and proliferation. Single-nucleotide polymorphisms in miRNA responsive elements within asthma susceptibility genes, and also in miRNAs themselves, can also contribute to the asthma phenotype. SUMMARY: Developing miRNA-based medicines to treat the pulmonary manifestations of asthma could yield therapeutics with new properties that have the potential to treat both the inflammation and hyperresponsivesness associated with this disease.


Subject(s)
Anti-Asthmatic Agents/pharmacology , Asthma/physiopathology , MicroRNAs/drug effects , MicroRNAs/physiology , Anti-Asthmatic Agents/therapeutic use , Asthma/drug therapy , Bronchi/pathology , Bronchi/physiopathology , Cell Proliferation , Disease Management , Genetic Predisposition to Disease/genetics , Humans , Polymorphism, Single Nucleotide/genetics
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