- importsource = "00280836-2010-06-10.txt"
- Artículo:
Control of mammary stem cell function by steroid hormone signalling
- Autor:
Marie-Liesse Asselin-Labat
François Vaillant
Julie M. Sheridan
Bhupinder Pal
Di Wu
Evan R. Simpson
Hisataka Yasuda
Gordon K. Smyth
T. John Martin
Geoffrey J. Lindeman
Jane E. Visvader
- Resumen:
The ovarian hormones oestrogen and progesterone increase breast cancer risk but the cellular mechanisms are unclear. Here it is shown that the size of the mammary stem cell pool in mice is regulated by steroid hormone signalling, although these cells lack the receptors for oestrogen and progesterone. The augmented pool could lead to clonal expansion of a mutated cell, possibly accounting for the increased incidence of breast cancer associated with pregnancy.
- Página:
798
- Publicación:
Nature
- Volúmen:
465
- Número:
7299
- Periodo:
10 Junio 2010
- ISSN:
00280836
- SrcID:
00280836-2010-06-10.txt
- Documento número 307781
- Actualizado el martes, 23 de mayo de 2017 03:58:18 p. m.
- Creado el martes, 23 de mayo de 2017 03:58:18 p. m.
- Enlace directo
- Artículo:
Progesterone induces adult mammary stem cell expansion
- Autor:
Purna A. Joshi
Hartland W. Jackson
Alexander G. Beristain
Marco A. Di Grappa
Patricia A. Mote
Christine L. Clarke
John Stingl
Paul D. Waterhouse
Rama Khokha
- Resumen:
Reproductive history influences breast cancer risk but the cellular mechanisms are unclear. Here it is shown that ovarian hormones regulate the size of the mammary stem cell pool in mice. The size of this pool increases when progesterone levels increase during the reproductive cycle. Progesterone probably regulates stem cell numbers through a paracrine mechanism involving induction of RANKL and Wnt in luminal cells.
- Página:
803
- Publicación:
Nature
- Volúmen:
465
- Número:
7299
- Periodo:
10 Junio 2010
- ISSN:
00280836
- SrcID:
00280836-2010-06-10.txt
- Documento número 307782
- Actualizado el martes, 23 de mayo de 2017 03:58:18 p. m.
- Creado el martes, 23 de mayo de 2017 03:58:18 p. m.
- Enlace directo
- Artículo:
Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome
- Autor:
Xonia Carvajal-Vergara
Ana Sevilla
Sunita L. D’Souza
Yen-Sin Ang
Christoph Schaniel
Dung-Fang Lee
Lei Yang
Aaron D. Kaplan
Eric D. Adler
Roye Rozov
YongChao Ge
Ninette Cohen
Lisa J. Edelmann
Betty Chang
Avinash Waghray
Jie Su
Sherly Pardo
Klaske D. Lichtenbelt
Marco Tartaglia
Bruce D. Gelb
Ihor R. Lemischka
- Resumen:
The generation of induced pluripotent stem cells (iPSCs) from patients with defined genetic disorders promises to help the basic understanding of complex diseases and the development of therapeutics. Here iPSCs have been generated from patients with LEOPARD syndrome, a developmental disorder with pleiomorphic effects on several tissues and organs. The iPSCs are characterized and the phenotype of cardiomyocytes derived from these cells is investigated.
- Página:
808
- Publicación:
Nature
- Volúmen:
465
- Número:
7299
- Periodo:
10 Junio 2010
- ISSN:
00280836
- SrcID:
00280836-2010-06-10.txt
- Documento número 307783
- Actualizado el martes, 23 de mayo de 2017 03:58:18 p. m.
- Creado el martes, 23 de mayo de 2017 03:58:18 p. m.
- Enlace directo
- Artículo:
Tumour angiogenesis is reduced in the Tc1 mouse model of Down’s syndrome
- Autor:
Louise E. Reynolds
Alan R. Watson
Marianne Baker
Tania A. Jones
Gabriela D’Amico
Stephen D. Robinson
Carine Joffre
Sarah Garrido-Urbani
Juan Carlos Rodriguez-Manzaneque
Estefanía Martino-Echarri
Michel Aurrand-Lions
Denise Sheer
Franca Dagna-Bricarelli
Dean Nizetic
Christopher J. McCabe
Andrew S. Turnell
Stephanie Kermorgant
Beat A. Imhof
Ralf Adams
Elizabeth M. C. Fisher
Victor L. J. Tybulewicz
Ian R. Hart
Kairbaan M. Hodivala-Dilke
- Resumen:
Down's syndrome is caused by trisomy of chromosome 21, and it is known that the growth of certain tumours is reduced in this genetic disorder. Using a mouse model of Down's syndrome, several individual genes on chromosome 21 are now being proposed to mediate the effect on tumour growth and angiogenesis.
- Página:
813
- Publicación:
Nature
- Volúmen:
465
- Número:
7299
- Periodo:
10 Junio 2010
- ISSN:
00280836
- SrcID:
00280836-2010-06-10.txt
- Documento número 307784
- Actualizado el martes, 23 de mayo de 2017 03:58:18 p. m.
- Creado el martes, 23 de mayo de 2017 03:58:18 p. m.
- Enlace directo
- Artículo:
Structural basis for 5?-nucleotide base-specific recognition of guide RNA by human AGO2
- Autor:
Filipp Frank
Nahum Sonenberg
Bhushan Nagar
- Resumen:
The association of microRNAs with Argonaute proteins (AGOs) yields complexes regulating gene expression. Although bacterial and archaeal miRNAs show no sequence preference at their 5? ends, eukaryotic miRNAs tend to have a 5? U or A. Here the structure of the human AGO2 MID domain complexed with ribonucleotide monophosphates is solved, revealing specific interaction of UMP and AMP with a loop that discriminates against CMP or GMP, and explaining the observed preference.
- Página:
818
- Publicación:
Nature
- Volúmen:
465
- Número:
7299
- Periodo:
10 Junio 2010
- ISSN:
00280836
- SrcID:
00280836-2010-06-10.txt
- Documento número 307785
- Actualizado el martes, 23 de mayo de 2017 03:58:18 p. m.
- Creado el martes, 23 de mayo de 2017 03:58:18 p. m.
- Enlace directo