Next: Andrea Califano, Columbia "De novo assembly... of regulatory networks reveals mechanism of tumorigenesis and chemosensitivity" #AACR14

4:37pm April 6th 2014 via Hootsuite

Sanford Simon: 'Encourage kids to ask questions about the world around them' 'Now I come home and discuss the science we're doing' #AACR14

4:32pm April 6th 2014 via Hootsuite

Elana Simon from AM (connection probs): 'Parents have emailed me about their kids' interest in science. I encourage them.' #AACR14

4:30pm April 6th 2014 via Hootsuite

Elana Simon: 'Publishing in Science still hasn't hit me'.'So many people around the world do not know about these (pt) communities' #AACR14

4:29pm April 6th 2014 via Hootsuite

From this morning: "I was amazed to see how much data was available." "Such a collaborative open project like this." Elana Simon #AACR14

4:27pm April 6th 2014 via Hootsuite

Permutter: Looking at TCGA mutational freq. data - can revisit the concept of immune surveillance. Immune response ‘sculpts’ tumors #AACR14

3:43pm April 6th 2014 via Hootsuite

Permutter: ‘We are encourage and intimidates sat the se time’ - so many agonists and antagonists on The T-cell surface #AACR14

3:39pm April 6th 2014 via Hootsuite

Permutter:Work on PD1 published in JCO Topalian et al. Last month, although not randomized study #AACR14

3:35pm April 6th 2014 via Hootsuite

Permutter: PD-1 an activation antigen on T and B cells; cancers can ‘hijack’ the PD1 pathway. Nivolumab targets PD1. #AACR14

3:33pm April 6th 2014 via Hootsuite

Permutter: Tumors have a way to inactivate T-cells. Illustrates immune checkpt regulation. #AACR14

3:31pm April 6th 2014 via Hootsuite

Permutter: at here must have been local T-cells that were recruited by the VTEC-induced antigen #AACR14

3:30pm April 6th 2014 via Hootsuite

Permutter: Showed efficacy of their viral vector with engineered antigen, incl ‘action at a distance’ #AACR14

3:28pm April 6th 2014 via Hootsuite

Permutter: Process of immunization: APC’s recruited, can increase amount of antigen ‘and it works’ #AACR14

3:24pm April 6th 2014 via Hootsuite

Permutter: Another option to expand CD19-reactive chimeric TCR-bearing T-cell clones that persist #AACR14

3:22pm April 6th 2014 via Hootsuite

Permutter: Bispecific Ab reagents to activate T-cells, other against tumor-assoc’d antigen. Redirected lysis #AACR14

3:19pm April 6th 2014 via Hootsuite

Permutter: Timeline include 2010 1st cellular immuno therapy (Provenge, prostate ca), 2011 anti-CTLA-4 #AACR14

3:16pm April 6th 2014 via Hootsuite

Permutter: An old field: 40y ago he looked at cell-mediated immunity. Timeline: enthusiasm (78-85), skepticism (85-97), renaissance #AACR14

3:14pm April 6th 2014 via Hootsuite

Up next: Roger Perlmutter, Merck. “Tumor-specific immune activation: immuno-oncology comes of age” #AACR14

3:09pm April 6th 2014 via Hootsuite

Willett: Weight gain as high a risk factor as for smoking for breast cancer in women. #AACR14

2:56pm April 6th 2014 via Hootsuite

Prives: ~1K genes affected by mut p53: is there a common mechanism? Do diff mutants affect invasion, migration, metastasis? #AACR14

1:17pm April 6th 2014 via Hootsuite

Prives: Suggests that mutant p53 drives expression of sterol biosynthesis enzymes SREBPs Ref from 2007: http://t.co/BxO5MKzpyD #AACR14

1:14pm April 6th 2014 via Hootsuite

Prives: Mevalonate pathway - affected by statins. Affect br ca cell growth? Showed morphology changes of disrupted p53 cells #AACR14

1:11pm April 6th 2014 via Hootsuite

Prives: Depletion of mutant p53 also down-regulated mevalonate pathway (cholesterol synthesis) #AACR14

1:08pm April 6th 2014 via Hootsuite

Prives: Using hu mammary MCF10A cells in 3D culture; induce shRNA-mediated knock-down the mutant p53; morphology became more normal #AACR14

1:07pm April 6th 2014 via Hootsuite

RT @BertGold4: Here is Young's NIH talk from a few months ago on super enhancers: http://t.co/cAF7yfczkx#AACR14 from far away..

1:03pm April 6th 2014 via Hootsuite

Prives: Tumor-derived missense mutated p53, led to the idea of mutant p53 confer gain-of-function #AACR14

1:00pm April 6th 2014 via Hootsuite

Prives: Extent of p53 mutations, refers to her Cell 2009 review: http://t.co/udCNnd8SoQ #AACR14

12:58pm April 6th 2014 via Hootsuite

Prives: p53 one of the most extensively-studied proteins. MdmX & Mdm2 supress it; multiple cellular outcomes once activated #AACR14

12:55pm April 6th 2014 via Hootsuite

Up next: Carol Prives, Columbia. “The two faces of p53: Tumor suppressor and oncogene” #AACR14

12:54pm April 6th 2014 via Hootsuite

.@teamoncology In yesterday's session Rosenfeld (UCSD) suggested Pit1 R27W mutation could become a target #AACR14

12:52pm April 6th 2014 via Hootsuite in reply to

RT @GenomeNathan: Young: cMyc saturation of enhancers drives promiscuous expression of relevant genes. #aacr14

12:48pm April 6th 2014 via Hootsuite

Young: Binding cooperativity on xcr - super enh ultra-sens. +JQ1 treatment impact on BRD4 2013 Cell ref: http://t.co/R6eBVOe1VP #AACR14

12:47pm April 6th 2014 via Hootsuite

Young: Super-enhancers suggest high c-Myc help recruit for pause-release 2012 Cell paper: http://t.co/Jrm4YBAmSN #AACR14

12:44pm April 6th 2014 via Hootsuite

Young: Super-anhancers haven't been noticed before as they drive mRNA with short half-life at a high level #AACR14

12:40pm April 6th 2014 via Hootsuite

Young: Tumor super-enhancers are at key genes (MYC, IGLL5) and acquired by oncogenes. Their 2013 Cell review http://t.co/DunSdVWJTW #AACR14

12:39pm April 6th 2014 via Hootsuite

RT @00livier: RY: 20-40% of the regulatory machinery binds to ~200 super enhancers #AACR14

12:35pm April 6th 2014 via Hootsuite

Young: Cell ID controlled by master TF's, first-gen maps of transcriptional control circuitry have begun #AACR14

12:34pm April 6th 2014 via Hootsuite

Young: DNA methylation, nucleosome mods (Ac, Me, Ub, Su), nucleosome mobilization, then stereotypical patterns of histone marks #AACR14

12:33pm April 6th 2014 via Hootsuite

Young: Master TF's - occupy their own gene expression. A 'core auto-regulatory loop'. Figure from Cell 2013 paper #AACR14

12:32pm April 6th 2014 via Hootsuite

Plenary session: Richard Young, MIT / Whitehead "Transcriptional and epigenetic control of tumor cells{" #AACR14

12:23pm April 6th 2014 via Hootsuite

Cancer patient, to survivor, to cancer researcher Elana Simon's story as video. Dad is Rockefeller U cancer researcher #AACR14

12:00pm April 6th 2014 via Hootsuite

Dr. Hanahan's 2 seminal 'must-read' papers 'for anyone entering the field'. '11: http://t.co/szOmbRxZFH '00: http://t.co/4ed2qG2rCA #AACR14

11:52am April 6th 2014 via Hootsuite

Great job from the #AACR organizers with opening video. I've seen a lot of great Big Corporation ones, this one is right up there! #AACR14

11:24am April 6th 2014 via Hootsuite

Ken Burns will be doing 'Emporer of All Maladies' as an upcoming PBS special http://t.co/6tSU1FRiqZ #AACR14

11:19am April 6th 2014 via Hootsuite

Friend: A2:Inst. - felt that most institutions are afraid that others know what they are really doing. A trust in the lab -> Inst. #AACR1

10:59am April 6th 2014 via Hootsuite

Friend:Q:Wall of q's - why inst. instead of crowdsourced? A:Use Stack Overflow so people can look at Q, then data, then fund it #AACR14

10:57am April 6th 2014 via Hootsuite

Friend:Q:Elemental public health issues: how to begin to use extremes? A:Hope to find 1M people to send info. Had 20K goal, hit 500K #AACR14

10:55am April 6th 2014 via Hootsuite

Friend:Q:Can it expand wide, how long to take? A:DARPA's Arpanet was for data; took only 20y to evolve. Feedback loop: faster &wider #AA

10:53am April 6th 2014 via Hootsuite

Friend:Q:Framing as computation, become shallow, 'relax' after they are on top? A:Agreed, need for experts work together after #AACR14

10:51am April 6th 2014 via Hootsuite

Friend: A2: What works well is to integrate with 'new experts'. A need for editors - to coordinate efforts #AACR14

10:49am April 6th 2014 via Hootsuite