OT: cell lines and tissues
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Rohit Ghai ▴ 80
@rohit-ghai-822
Last seen 9.6 years ago
hi Stefan I feel that such comparisons would not offer as much contrast and clarity. Normal tissues would be best, even if isolation is tedious. Cell lines grow in a completely different environment than tissues. Gene expression is critically dependent on outside cues from other cells in the tissue too. Of course, this also depends on what is the question you are asking. If its a question of identifying markers, these may be identified as one can then verify individual markers on a smaller scale. But for a better distinction of the processes underlying the disease state it would be better to use normal ovarian epithelium. regards Rohit ------------------------------------------------------------------ Hi everybody. This is definitely Off-Topic, but I'd like to have an opinion from the many biologist (but not only!) that populate the list, about the following problem: A group of biologists is willing to study gene expression in ovarian cancer tissues relative to normal ones. As the normal ovarian epithelium is single layer, it's quite hard to get enough RNA. So they are actually going to compare normal ovarian cell lines grown in vitro versus patological tissues. I feel a bit confused about this. Wouldn't be better to amplify the RNA from normal tissues? Any other options? Any insight will be very appreciated. TIA, Stefano
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@stecalzatiscaliit-259
Last seen 9.6 years ago
Hi Rohit, this was my point. But their (and mine at the statistical analysis step) problem is that from the normal tissue itself they cannot collect enough RNA. Then, what could be the best (or least bad) solution? Microdissection would bring into the normal sample a mixture of cells, not only epithelial ones. Amplifying RNA from the normal tissue (they already have the chips for th patholigical ones) would probably bias the expression, though I guess the overall expression (or also differentially at gene level?). Summarizing: what could be the best procedure? TIA, Stefano On Tue, Jul 06, 2004 at 08:18:13PM +0200, Ghai, Rohit wrote: > hi Stefan > > I feel that such comparisons would not offer as much contrast > and clarity. Normal tissues would be best, even if isolation > is tedious. Cell lines grow in a completely different environment > than tissues. Gene expression is critically dependent on outside > cues from other cells in the tissue too. Of course, this also depends on > what is the question you are asking. If its a question of identifying > markers, these may be identified as one can then verify individual markers > on a smaller scale. But for a better distinction of the processes underlying > the disease state it would be better to use normal ovarian epithelium. > > regards > Rohit > > ------------------------------------------------------------------ > Hi everybody. > > This is definitely Off-Topic, but I'd like to have an opinion from the many > biologist (but not only!) that populate the list, about the following > problem: > > A group of biologists is willing to study gene expression in ovarian cancer > tissues relative to normal ones. As the normal ovarian epithelium is single > layer, it's quite hard to get enough RNA. So > > they are actually going to compare normal ovarian cell lines grown in vitro > versus patological tissues. I feel a bit confused about this. Wouldn't be > better to amplify the RNA from normal > > tissues? Any other options? > > Any insight will be very appreciated. > > TIA, > Stefano > > _______________________________________________ > Bioconductor mailing list > Bioconductor@stat.math.ethz.ch > https://www.stat.math.ethz.ch/mailman/listinfo/bioconductor
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Dapeng Cui ▴ 40
@dapeng-cui-463
Last seen 9.6 years ago
My suggestion is to do microdissection and amplify both tissues starting from the same amount of RNA/cells. Dapeng Cui >>> Stefano Calza <stecalza@tiscali.it> 07/07/04 08:02AM >>> Hi Rohit, this was my point. But their (and mine at the statistical analysis step) problem is that from the normal tissue itself they cannot collect enough RNA. Then, what could be the best (or least bad) solution? Microdissection would bring into the normal sample a mixture of cells, not only epithelial ones. Amplifying RNA from the normal tissue (they already have the chips for th patholigical ones) would probably bias the expression, though I guess the overall expression (or also differentially at gene level?). Summarizing: what could be the best procedure? TIA, Stefano On Tue, Jul 06, 2004 at 08:18:13PM +0200, Ghai, Rohit wrote: > hi Stefan > > I feel that such comparisons would not offer as much contrast > and clarity. Normal tissues would be best, even if isolation > is tedious. Cell lines grow in a completely different environment > than tissues. Gene expression is critically dependent on outside > cues from other cells in the tissue too. Of course, this also depends on > what is the question you are asking. If its a question of identifying > markers, these may be identified as one can then verify individual markers > on a smaller scale. But for a better distinction of the processes underlying > the disease state it would be better to use normal ovarian epithelium. > > regards > Rohit > > ------------------------------------------------------------------ > Hi everybody. > > This is definitely Off-Topic, but I'd like to have an opinion from the many > biologist (but not only!) that populate the list, about the following > problem: > > A group of biologists is willing to study gene expression in ovarian cancer > tissues relative to normal ones. As the normal ovarian epithelium is single > layer, it's quite hard to get enough RNA. So > > they are actually going to compare normal ovarian cell lines grown in vitro > versus patological tissues. I feel a bit confused about this. Wouldn't be > better to amplify the RNA from normal > > tissues? Any other options? > > Any insight will be very appreciated. > > TIA, > Stefano > > _______________________________________________ > Bioconductor mailing list > Bioconductor@stat.math.ethz.ch > https://www.stat.math.ethz.ch/mailman/listinfo/bioconductor _______________________________________________ Bioconductor mailing list Bioconductor@stat.math.ethz.ch https://www.stat.math.ethz.ch/mailman/listinfo/bioconductor
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Rohit Ghai ▴ 80
@rohit-ghai-822
Last seen 9.6 years ago
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Hi. I want to use expresso to apply RMA with VSN normalization. I use the following code: expresso(dati,normalize.method="vsn",bgcorrect.method="rma",pmcorrect. method="pmonly",summary.method="medianpolish") Every is fine but when I get to ... ... normalizing...vsn: [skipped]: Error: L-BFGS-B needs finite values of fn What's wrong? TIA, Stefano
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YUK FAI LEUNG ▴ 140
@yuk-fai-leung-605
Last seen 9.6 years ago
Dear Stefano, Why don't you use both of them as controls? A group of RNAs from normal amplified RNA from tissue, and a group of RNAs from cell lines. Then you can make more comparisons! Best regards, Fai ------- Hi everybody. This is definitely Off-Topic, but I'd like to have an opinion from the many biologist (but not only!) that populate the list, about the following problem: A group of biologists is willing to study gene expression in ovarian cancer tissues relative to normal ones. As the normal ovarian epithelium is single layer, it's quite hard to get enough RNA. So they are actually going to compare normal ovarian cell lines grown in vitro versus patological tissues. I feel a bit confused about this. Wouldn't be better to amplify the RNA from normal tissues? Any other options? Any insight will be very appreciated. TIA, Stefano -- Yuk Fai Leung Department of Molecular and Cellular Biology Harvard University BL 2079, 16 Divinity Avenue Cambridge, MA 02138 Tel: 617-495-2599 Fax: 617-496-3321 email: yfleung@mcb.harvard.edu; yfleung@genomicshome.com URL: http://genomicshome.com
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