BMC Cancer

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Open Access Research article

Repeated BCG treatment of mouse bladder selectively stimulates small GTPases and HLA antigens and inhibits single-spanning uroplakins

Marcia R Saban1, Helen L Hellmich2, Cindy Simpson1, Carole A Davis1, Mark L Lang3, Michael A Ihnat4, Michael A O'Donnell5, Xue-Ru Wu6 and Ricardo Saban1*

Author Affiliations

1 Department of Physiology, The University Oklahoma Health Sciences Center, Oklahoma City, USA

2 Department of Anesthesiology, University of Texas Medical Branch, Galveston, USA

3 Department of Microbiology and Immunology The University Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA

4 Department of Cell Biology, The University Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA

5 Department of Urology, University of Iowa, UI Hospitals and Clinics, Iowa City, Iowa 52242-1089, USA

6 Department of Urology, New York University, School of Medicine, New York, NY 10016, USA

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BMC Cancer 2007, 7:204 doi:10.1186/1471-2407-7-204

Published: 2 November 2007

Additional files

Additional file 1:

Agarose gel electrophoresis of RNA samples. C = saline-treated and T=BCG-treated.

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Additional file 2:

Agarose gel electrophoresis of ds cDNA synthesis and Rsa I digestion. Lane 1-SMART-amplified C cDNA (driver); Lane 2-SMART-amplified T cDNA (tester); Lane 3-Rsa I digested C cDNA; and Lane 4-Rsa I digested T cDNA M = 1 kb DNA size markers.

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Additional file 3:

Table 1 Oligonucleotides used

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Additional file 4:

Agarose gel electrophoresis of primary and secondary PCR products. Lane M = 1 kb DNA size markers, Lane 1 = primary PCR of C subtracted cDNA; Lane 2 = primary PCR of T subtracted cDNA; Lane 3 = secondary PCR of C subtracted cDNA; Lane 4 = secondary PCR of T subtracted cDNA; Lane 5 = unsubtracted C cDNA; and Lane 6 = unsubtracted T cDNA.

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Additional file 5:

Table 2. QOCR Primers

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Additional file 6:

Differential screening of plate C-1 from C (driver) subtracted library was subjected to differential screening using driver-specific (A) and tester-specific (B) subtracted probes.

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Additional file 7:

Differential screening of plate C-2 from C (driver) subtracted library was subjected to differential screening using driver-specific (A) and tester-specific (B) subtracted probes.

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Additional file 8:

Differential screening of plate T-1 from T (tester) subtracted library was subjected to differential screening using driver-specific (A) and tester-specific (B) subtracted probes.

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Additional file 9:

Differential screening of plate T-2 from T (tester) subtracted library was subjected to differential screening using driver-specific (A) and tester-specific (B) subtracted probes.

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Additional file 10:

Differential screening of plate T-3 from T (tester) subtracted library was subjected to differential screening using driver-specific (A) and tester-specific (B) subtracted probes.

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Additional file 11:

Differential screening of plate T-4 from T (tester) subtracted library was subjected to differential screening using driver-specific (A) and tester-specific (B) subtracted probes.

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Additional file 12:

Differential screening of plate T-5 from T (tester) subtracted library was subjected to differential screening using driver-specific (A) and tester-specific (B) subtracted probes.

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Additional file 13:

Virtual Northern blot analysis of differential clones obtained from control bladder (C) subtracted library. A = Plate C-1 and B = Plate C-2

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Additional file 14:

Virtual Northern blot analysis of differential clones obtained from BCG-treated bladder (T) subtracted library. A = Plate T-1; B = Plate T-2; C = Plate T-3; D = Plate T-4; and E = Plate T-5.

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Additional file 15:

Table 3. Genes up-regulated by BCG

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Additional file 16:

Table 4. Genes down-regulated by BCG.

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Additional file 17:

Table 5. Ingenuity Summary BCG.

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Additional file 18:

Table 6. Ingenuity Summary Control.

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