نتایج جستجو برای: rhabdomyosarcoma

تعداد نتایج: 21356  

Journal: :Annals of African medicine 2007
A Shayah F O Agada L Karsai N Stafford

Rhabdomyosarcoma is relatively seen in the pediatric age group with the head and neck region as the commonest site. To the best of our knowledge, few cases of laryngeal involvement in adult have been described in the literature. Biologically, rhabdomyosarcoma is different from squamous cell carcinoma, which is the commonest tumor of the larynx. A previously healthy non-smoker 77-year-old lady p...

2012
Paolo Romania Alice Bertaina Giorgia Bracaglia Franco Locatelli Doriana Fruci Rossella Rota

Gene expression control mediated by microRNAs and epigenetic remodeling of chromatin are interconnected processes often involved in feedback regulatory loops, which strictly guide proper tissue differentiation during embryonal development. Altered expression of microRNAs is one of the mechanisms leading to pathologic conditions, such as cancer. Several lines of evidence pointed to epigenetic al...

Journal: :Journal of the Egyptian National Cancer Institute 2005
Tarek Shouman Ihab El-Kest Khalid Zaza Mohamad Ezzat Hany William Ibrahim Ezzat

OBJECTIVES The study goal was to retrospectively review the treatment results of childhood rhabdomyosarcoma and identify prognostic factors that affect treatment outcome. PATIENTS AND METHODS The records of 190 patients with childhood rhabdomyosarcoma treated between January 1991 and December 1999 were reviewed. The data were analyzed for clinico-epidemiological factors and the impact of pote...

2014
Juan Huertas-Martínez Santiago Rello-Varona David Herrero-Martín Ignasi Barrau Silvia García-Monclús Miguel Sáinz-Jaspeado Laura Lagares-Tena Yaiza Núñez-Álvarez Silvia Mateo-Lozano Jaume Mora Josep Roma Nuria Toran Sebastian Moran Roser López-Alemany Soledad Gallego Manel Esteller Miguel A. Peinado Muro Xavier García del Oscar M. Tirado

Rhabdomyosarcoma is the most common soft tissue sarcoma of childhood and adolescence. Despite advances in therapy, patients with histological variant of rhabdomyosarcoma known as alveolar rhabdomyosarcoma (ARMS) have a 5-year survival of less than 30%. Caveolin-1 (CAV1), encoding the structural component of cellular caveolae, is a suggested tumor suppressor gene involved in cell signaling. In t...

Journal: :journal of current ophthalmology 0
yungang ding hehua ye hehua ye huijing ye huasheng yang

dear editor:   we thank dr asadi amoli for her interest in our article. 1 dr asadi amoli pointed out that specific and sensitive rhabdomyosarcoma (rms) markers should be investigated in our case. 2 we agree with dr asadi amoli ’s opinion and are sorry that the results of pathology examination and myogenin (myf-4) staining studied in a local hospital were not provided in our case report.   an ex...

Journal: :Molecular cancer therapeutics 2009
Kaiji Hu Cathy Lee Dexin Qiu Abbas Fotovati Alastair Davies Samah Abu-Ali Daniel Wai Elizabeth R Lawlor Timothy J Triche Catherine J Pallen Sandra E Dunn

Rhabdomyosarcoma, consisting of alveolar (aRMS) and embryonal (eRMS) subtypes, is the most common type of sarcoma in children. Currently, there are no targeted drug therapies available for rhabdomyosarcoma. In searching for new molecular therapeutic targets, we carried out genome-wide small interfering RNA (siRNA) library screens targeting human phosphatases (n = 206) and kinases (n = 691) init...

Journal: :Transactions of the American Ophthalmological Society 2001
C L Shields J A Shields S G Honavar H Demirci

PURPOSE To review the findings, management, and outcome in 33 cases of primary ophthalmic rhabdomyosarcoma. METHODS The records of 33 consecutive patients from a single ocular oncology center were analyzed retrospectively for outcomes of final visual acuity, local recurrence, and distant metastasis. RESULTS Rhabdomyosarcoma was primarily located in the orbit m 25 cases (76%), conjunctiva in...

Journal: :Indian pediatrics 2017
Deepak Bansal Anirban Das Amita Trehan Rakesh Kapoor Naresh K Panda Radhika Srinivasan Nandita Kakkar Kushaljit S Sodhi Akshay K Saxena Katragadda Lakshmi Narasimha Rao

OBJECTIVE Analyze the profile and outcome of children with rhabdomyosarcoma from a pediatric-oncology unit. DESIGN Retrospective analysis of case records over 23 years (1990-2012). Setting Government-run, tertiary-care, university hospital in Northern India. PARTICIPANTS 159 children (<12-years) with a diagnosis of rhabdomyosarcoma were enrolled. The median age was 4 years; 13% were infan...

Journal: :Folia histochemica et cytobiologica 2010
Katarzyna Miekus Danuta Jarocha Elzbieta Trzyna Marcin Majka

Chemokines and its receptors stimulate tumor growth, migration and invasion. In this study we evaluated the expression and function of CXCR3 and CXCR7 receptors in cervical carcinoma, rhabdomyosarcoma and glioblastoma cell lines. We found that both receptors were expressed at different degree by tumor cells. CXCR7 was expressed at both mRNA and protein level by all tumor cell lines. The express...

Journal: :The Journal of clinical investigation 2009
Adam D Durbin Gino R Somers Michael Forrester Malgorzata Pienkowska Gregory E Hannigan David Malkin

Although most reports describe the protein kinase integrin-linked kinase (ILK) as a proto-oncogene, occasional studies detail opposing functions in the regulation of normal and transformed cell proliferation, differentiation, and apoptosis. Here, we demonstrated that ILK functions as an oncogene in the highly aggressive pediatric sarcoma alveolar rhabdomyosarcoma (ARMS) and as a tumor suppresso...

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