PENUAAN FIBROBLAS KELOID OLEH TRIAMSINOLON ASETONIDA ATAU MITOMISIN C

The defective induction of senescence may provoke keloid. Therapy that induces fibroblasts senescence can be used to prevent the keloid. Triamcinolon acetonide (TA) or Mitomycin C (MMC) can improve keloid by decreasing fibroblasts proliferation that is also the characteristic of cellular senescence....

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Main Authors: , dr. Marta Dwi Rifka, , dr. Y. Widodo Wirohadidjojo, Sp.KK(K)
Format: Thesis
Published: [Yogyakarta] : Universitas Gadjah Mada 2011
Subjects:
ETD
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author , dr. Marta Dwi Rifka
, dr. Y. Widodo Wirohadidjojo, Sp.KK(K)
author_facet , dr. Marta Dwi Rifka
, dr. Y. Widodo Wirohadidjojo, Sp.KK(K)
author_sort , dr. Marta Dwi Rifka
collection UGM
description The defective induction of senescence may provoke keloid. Therapy that induces fibroblasts senescence can be used to prevent the keloid. Triamcinolon acetonide (TA) or Mitomycin C (MMC) can improve keloid by decreasing fibroblasts proliferation that is also the characteristic of cellular senescence. We investigated the effect of TA or MMC on SA-βgal senescence-marker expression of keloid fibroblasts, the optimum dose of TA or MMC and the potential difference in increasing the expression between the use of TA and MMC. Passage III keloid fibroblasts culture was divided into 8 groups of treatment: placebo, 150 µM H2O2 (as procedure control), TA (10, 20, 40 µM), and MMC (0,015
first_indexed 2024-03-13T22:09:43Z
format Thesis
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institution Universiti Gadjah Mada
last_indexed 2024-03-13T22:09:43Z
publishDate 2011
publisher [Yogyakarta] : Universitas Gadjah Mada
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spelling oai:generic.eprints.org:902182014-08-20T02:54:36Z https://repository.ugm.ac.id/90218/ PENUAAN FIBROBLAS KELOID OLEH TRIAMSINOLON ASETONIDA ATAU MITOMISIN C , dr. Marta Dwi Rifka , dr. Y. Widodo Wirohadidjojo, Sp.KK(K) ETD The defective induction of senescence may provoke keloid. Therapy that induces fibroblasts senescence can be used to prevent the keloid. Triamcinolon acetonide (TA) or Mitomycin C (MMC) can improve keloid by decreasing fibroblasts proliferation that is also the characteristic of cellular senescence. We investigated the effect of TA or MMC on SA-βgal senescence-marker expression of keloid fibroblasts, the optimum dose of TA or MMC and the potential difference in increasing the expression between the use of TA and MMC. Passage III keloid fibroblasts culture was divided into 8 groups of treatment: placebo, 150 µM H2O2 (as procedure control), TA (10, 20, 40 µM), and MMC (0,015 [Yogyakarta] : Universitas Gadjah Mada 2011 Thesis NonPeerReviewed , dr. Marta Dwi Rifka and , dr. Y. Widodo Wirohadidjojo, Sp.KK(K) (2011) PENUAAN FIBROBLAS KELOID OLEH TRIAMSINOLON ASETONIDA ATAU MITOMISIN C. UNSPECIFIED thesis, UNSPECIFIED. http://etd.ugm.ac.id/index.php?mod=penelitian_detail&sub=PenelitianDetail&act=view&typ=html&buku_id=51186
spellingShingle ETD
, dr. Marta Dwi Rifka
, dr. Y. Widodo Wirohadidjojo, Sp.KK(K)
PENUAAN FIBROBLAS KELOID OLEH TRIAMSINOLON ASETONIDA ATAU MITOMISIN C
title PENUAAN FIBROBLAS KELOID OLEH TRIAMSINOLON ASETONIDA ATAU MITOMISIN C
title_full PENUAAN FIBROBLAS KELOID OLEH TRIAMSINOLON ASETONIDA ATAU MITOMISIN C
title_fullStr PENUAAN FIBROBLAS KELOID OLEH TRIAMSINOLON ASETONIDA ATAU MITOMISIN C
title_full_unstemmed PENUAAN FIBROBLAS KELOID OLEH TRIAMSINOLON ASETONIDA ATAU MITOMISIN C
title_short PENUAAN FIBROBLAS KELOID OLEH TRIAMSINOLON ASETONIDA ATAU MITOMISIN C
title_sort penuaan fibroblas keloid oleh triamsinolon asetonida atau mitomisin c
topic ETD
work_keys_str_mv AT drmartadwirifka penuaanfibroblaskeloidolehtriamsinolonasetonidaataumitomisinc
AT drywidodowirohadidjojospkkk penuaanfibroblaskeloidolehtriamsinolonasetonidaataumitomisinc