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Molecular Biology and Genetics

Gastric and Hepatocellular Carcinomas Do Not Overexpress the Same Ribosomal Protein Messenger RNAs as Colonic Carcinoma

Graham F. Barnard, Raymond J. Staniunas, Masaki Mori, Mark Puder, Milburn J. Jessup, Glenn D. Steele Jr. and Lan Bo Chen
Graham F. Barnard
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Raymond J. Staniunas
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Masaki Mori
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Mark Puder
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Milburn J. Jessup
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Glenn D. Steele Jr.
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Lan Bo Chen
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DOI:  Published September 1993
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Abstract

The levels of a number of ribosomal protein mRNAs are reported to be increased in human colon cancer. We have assessed whether selected ribosomal protein mRNAs are overexpressed in other gastrointestinal malignancies, namely gastric and hepatocellular carcinomas. Subtracted complementary DNA libraries were generated from paired samples of human (a) colorectal carcinoma minus adjacent normal colonic mucosa and (b) hepatocellular carcinoma minus adjacent normal liver. Screening of ∼3% of these library clones determined that ribosomal protein mRNAs encoding L18 and L37 (not previously reported) and P0 and S6 were overexpressed in one or the other library. Their complementary DNA inserts were then used as probes to evaluate their expression in a larger number of paired tumor/normal surgical samples of human colonic, gastric, and hepatocellular carcinomas, by Northern hybridization. The mRNA signal was greater in the colonic carcinoma than in paired adjacent normal colonic mucosa in 38 of 42 cases for P0 [tumor/normal (T/N) ratio = 3.0 ± 0.3, mean ± SE, P < 0.001] (G. F. Barnard, R. J. Staniunas, S. Bao, K. Mafune, J. L. Gollan, G. D. Steele, Jr., and L. B. Chen, Cancer Res., 52: 3067–3072, 1992), in 25 of 28 cases for L18 (T/N ratio = 3.7 ± 0.5, P < 0.001), in 27 of 28 cases for L37 (T/N ratio = 5.3 ± 0.4, P < 0.001), and in 24 of 28 cases for S6 (T/N ratio = 3.1 ± 0.5, P < 0.01). The level of mRNA overexpression of L18 and S6 did not correlate with the Dukes' stage of disease. In hepatocellular carcinoma samples, using the same four ribosomal protein complementary DNA probes, only P0 mRNA was significantly increased (T/N ratio = 2.8 ± 0.4, n = 6, P = 0.047). In gastric carcinoma samples, none of these mRNAs was increased (mean T/N ratios = 0.9-1.2, n = 6). Therefore, gastric and hepatocellular carcinomas do not overexpress the same ribosomal protein mRNAs as do colonic carcinoma.

Footnotes

  • ↵1 This work was supported by NIH Grants CA44704, DK07533, and NCI 5F32CA-0900. Presented in part at the annual meetings of the American College of Surgeons (San Francisco, CA, 1990) (1), the American Society of Cell Biology (Boston, MA, 1991) (2), and the American Gastroenterological Association (San Francisco, CA, 1992) (3).

  • ↵3 To whom requests for reprints should be addressed, at the Division of Cellular and Molecular Biology, Mayer 840, Dana-Farber Cancer Institute, 44 Binney St., Boston, MA 02115.

  • Received January 11, 1993.
  • Accepted June 21, 1993.
  • ©1993 American Association for Cancer Research.
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September 1993
Volume 53, Issue 17
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Gastric and Hepatocellular Carcinomas Do Not Overexpress the Same Ribosomal Protein Messenger RNAs as Colonic Carcinoma
Graham F. Barnard, Raymond J. Staniunas, Masaki Mori, Mark Puder, Milburn J. Jessup, Glenn D. Steele Jr. and Lan Bo Chen
Cancer Res September 1 1993 (53) (17) 4048-4052;

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Gastric and Hepatocellular Carcinomas Do Not Overexpress the Same Ribosomal Protein Messenger RNAs as Colonic Carcinoma
Graham F. Barnard, Raymond J. Staniunas, Masaki Mori, Mark Puder, Milburn J. Jessup, Glenn D. Steele Jr. and Lan Bo Chen
Cancer Res September 1 1993 (53) (17) 4048-4052;
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