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Comparison of Agar and Agarose Culture Methods for Human Tumor Stem Cell Assay of Gynecologic Tumors : 부인과 영역의 악성종양에 있어서 human tumor stem cell assay를 위한 agar배지와 agarose배지의 비교

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dc.contributor.authorLee, Hyo Pyo-
dc.contributor.authorCha, Sang Hun-
dc.date.accessioned2009-07-14T08:24:24Z-
dc.date.available2009-07-14T08:24:24Z-
dc.date.issued1986-06-
dc.identifier.citationSeoul J Med, Vol.27 No.2, pp. 169-172-
dc.identifier.issn0582-6802-
dc.identifier.urihttps://hdl.handle.net/10371/5505-
dc.description.abstractThe human tumor stem cell assay (HTSCA) has broad research applications in
the field of cell biology as well as in clinical chemotherapy. A prospective clinical trial for
improvement of the in vitro growth rate of gynecologic cancers was done between agar and
agarose culture methods. Specimens from 27 gynecologic tumors were disaggregated by
mechanical and enzymatic methods and assayed in soft agar and agarose culture matrix. 9 of
27 tumors grew in the agar system yielding a cloning success rate of 33.3%. Of 27 specimens,
17 have shown colony growth in the agarose culture matrix showing a cloning success rate of
63.0%. Cloning efficiency in agarose improved approximately 2-fold as compared with that in
agar. The development of a soft agarose assay for gynecologic tumor cells will provide a
possibility of an in vitro technique for predicting in vivo response to anticancer drugs.
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dc.language.isoen-
dc.publisherSeoul National University College of Medicine-
dc.subjectAgar-
dc.subjectAgarose-
dc.subjectClone Cells-
dc.subjectGynecologic Tumor-
dc.titleComparison of Agar and Agarose Culture Methods for Human Tumor Stem Cell Assay of Gynecologic Tumors-
dc.title.alternative부인과 영역의 악성종양에 있어서 human tumor stem cell assay를 위한 agar배지와 agarose배지의 비교-
dc.typeSNU Journal-
dc.contributor.AlternativeAuthor이효표-
dc.contributor.AlternativeAuthor차상헌-
dc.citation.journaltitle서울 의대 잡지-
dc.citation.journaltitle서울 의대 학술지-
dc.citation.journaltitleSeoul Journal of Medicine-
dc.citation.endpage172-
dc.citation.number2-
dc.citation.pages169-172-
dc.citation.startpage169-
dc.citation.volume27-
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