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3. Consensus guidelines for the use and interpretation of angiogenesis assays

Author

Nowak-Sliwinska, Patrycja, Alitalo, Kari, Allen, Elizabeth, Anisimov, Andrey, Aplin, Alfred C., Auerbach, Robert, Augustin, Hellmut G., Bates, David O., van Beijnum, Judy R., Bender, R. Hugh F., Bergers, Gabriele, Bikfalvi, Andreas, Bischoff, Joyce, Böck, Barbara C., Brooks, Peter C., Bussolino, Federico, Cakir, Bertan, Carmeliet, Peter, Castranova, Daniel, Cimpean, Anca M., Cleaver, Ondine, Coukos, George, Davis, George E., De Palma, Michele, Dimberg, Anna, Dings, Ruud P. M., Djonov, Valentin, Dudley, Andrew C., Dufton, Neil P., Fendt, Sarah-Maria, Ferrara, Napoleone, Fruttiger, Marcus, Fukumura, Dai, Ghesquière, Bart, Gong, Yan, Griffin, Robert J., Harris, Adrian L., Hughes, Christopher C. W., Hultgren, Nan W., Iruela-Arispe, M. Luisa, Irving, Melita, Jain, Rakesh K., Kalluri, Raghu, Kalucka, Joanna, Kerbel, Robert S., Kitajewski, Jan, Klaassen, Ingeborg, Kleinmann, Hynda K., Koolwijk, Pieter, Kuczynski, Elisabeth, Kwak, Brenda R., Marien, Koen, Melero-Martin, Juan M., Munn, Lance L., Nicosia, Roberto F., Noel, Agnes, Nurro, Jussi, Olsson, Anna-Karin, Petrova, Tatiana V., Pietras, Kristian, Pili, Roberto, Pollard, Jeffrey W., Post, Mark J., Quax, Paul H. A., Rabinovich, Gabriel A., Raica, Marius, Randi, Anna M., Ribatti, Domenico, Ruegg, Curzio, Schlingemann, Reinier O., Schulte-Merker, Stefan, Smith, Lois E. H., Song, Jonathan W., Stacker, Steven A., Stalin, Jimmy, Stratman, Amber N., Van de Velde, Maureen, van Hinsbergh, Victor W. M., Vermeulen, Peter B., Waltenberger, Johannes, Weinstein, Brant M., Xin, Hong, Yetkin-Arik, Bahar, Yla-Herttuala, Seppo, Yoder, Mervin C., and Griffioen, Arjan W.

Published
2018
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6. Activated K-Ras, but Not H-Ras or N-Ras, Regulates Brain Neural Stem Cell Proliferation in a Raf/Rb-Dependent Manner.

Author

Bender, R. Hugh F., Gutmann, David H., and Haigis, Kevin M.

Subjects
RAS proteins, NEURAL stem cells, CELL proliferation
Abstract

Neural stem cells (NSCs) give rise to all the major cell types in the brain, including neurons, oligodendrocytes, and astrocytes. However, the intracellular signaling pathways that govern brain NSC proliferation and differentiation have been incompletely characterized to date. Since some neurodevelopmental brain disorders (Costello syndrome and Noonan syndrome) are caused by germline activating mutations in the RAS genes, Ras small GTPases are likely critical regulators of brain NSC function. In the mammalian brain, Ras exists as three distinct molecules (H-Ras, K-Ras, and N-Ras), each with different subcellular localizations, downstream signaling effectors, and biological effects. Leveraging a novel series of conditional-activated Ras molecule-expressing genetically engineered mouse strains, we demonstrate that activated K-Ras, but not H-Ras or N-Ras, expression increases brain NSC growth in a Raf-dependent, but Mek-independent, manner. Moreover, we show that activated K-Ras regulation of brain NSC proliferation requires Raf binding and suppression of retinoblastoma (Rb) function. Collectively, these observations establish tissue-specific differences in activated Ras molecule regulation of brain cell growth that operate through a noncanonical mechanism. S tem C ells 2015;33:1998-2010 [ABSTRACT FROM AUTHOR]

Published
2015
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7. Identification of a Novel TP53 Cancer Susceptibility Mutation Through Whole-Genome Sequencing of a Patient With Therapy-Related AML.

Author

Link, Daniel C., Schuettpelz, Laura G., Dong Shen, Jinling Wang, Walter, Matthew J., Kulkarni, Shashikant, Payton, Jacqueline E., Ivanovich, Jennifer, Goodfellow, Paul J., Le Beau, Michelle, Koboldt, Daniel C., Dooling, David J., Fulton, Robert S., Bender, R. Hugh F., Fulton, Lucinda L., Delehaunty, Kimberly D., Fronick, Catrina C., Appelbaum, Elizabeth L., Schmidt, Heather, and Abbott, Rachel

Subjects
NUCLEOTIDE sequence, CANCER susceptibility, TUMORS, GERM cells, BONE marrow cells, GENETIC polymorphisms
Abstract

The article discusses a study that applies whole-genome sequencing to a patient who had no significant family history of cancer but who had a suspected higher cancer susceptibility due to multiple primary tumors, with the aim of identifying rare or novel germline variants in cancer susceptibility genes. Skin and bone marrow DNA were acquired from the cancer patient. The samples were analyzed with whole-genome sequencing using paired-end reads, single-nucleotide polymorphism (SNP) genotyping, spectral karyotyping and RNA expression profiling.

Published
2011
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