Staurosporine-induced apoptosis is independent of p16 and p21 and achieved via arrest at G2/M and at G1 in U251MG human glioma cell line (Q40651329)

22 September 2017

title

Staurosporine-induced apoptosis is independent of p16 and p21 and achieved via arrest at G2/M and at G1 in U251MG human glioma cell line (English)

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22 September 2017

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https://api.crossref.org/works/10.1007/S00280-002-0562-Z

29 December 2023

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https://api.crossref.org/works/10.1007/S00280-002-0562-Z

29 December 2023

1

Fumiyuki Yamasaki

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12721754

29 December 2023

author name string

Seiji Hama

2

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22 September 2017

Hiroyuki Yoshioka

3

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22 September 2017

Yoshinori Kajiwara

4

1 reference

22 September 2017

Kaita Yahara

5

1 reference

22 September 2017

Kazuhiko Sugiyama

6

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22 September 2017

Yuji Heike

7

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22 September 2017

Kazunori Arita

8

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22 September 2017

Kaoru Kurisu

9

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22 September 2017

language of work or name

Englisch

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12721754

29 December 2023

publication date

20 March 2003

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Cancer Chemotherapy and Pharmacology

22 September 2017

published in

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22 September 2017

volume

51

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22 September 2017

issue

4

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22 September 2017

page(s)

271-283

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Highly synchronous culture of fibroblasts from G2 block caused by staurosporine, a potent inhibitor of protein kinases

22 September 2017

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Mitochondrial cytochrome c release in apoptosis occurs upstream of DEVD-specific caspase activation and independently of mitochondrial transmembrane depolarization.

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Protein kinase C inhibition by UCN-01 induces apoptosis in human glioma cells in a time-dependent fashion

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Characterization of receptor tyrosine-specific protein kinases by the use of inhibitors. Staurosporine is a 100-times more potent inhibitor of insulin receptor than IGF-I receptor.

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Human wee1 maintains mitotic timing by protecting the nucleus from cytoplasmically activated Cdc2 kinase

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Cdc2 activation is not required for thymocyte apoptosis

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Identifiers

Dimensions Publication ID

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1075277728

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1 reference