Skip to main content
Log in

Aberrations of theAPC gene in primary breast carcinoma

  • Original Papers
  • Clinical Oncology
  • Published:
Journal of Cancer Research and Clinical Oncology Aims and scope Submit manuscript

Abstract

Aberrations of theAPC gene, which plays an important role in the genesis of familial adenomatous polyposis and colorectal carcinoma, were investigated in 31 surgical specimens of primary breast carcinoma. These studies utilized the polymerase chain reaction followed by restriction-fragment-length polymorphism and single-strand-conformation polymorphism analyses combined with tumor cell enrichment by cell sorting. Loss of heterozygosity at theAPC locus was detected in 8 (38%) of 21 informative cases, but only 2 (6%) of 31 tumors carried a mutatedAPC gene. Direct DNA sequencing analysis confirmed mutations at codon 1081 (AGC to ATC) resulting in an amino acid substitution of serine for isoleucine, and at codon 1096 (CAG to CAT) resulting in a substitution of glutamine for histidine. There were no significant correlations between the loss of heterozygosity or mutation at theAPC locus and any clinicopathological characteristics. Our present observations suggest that the mutations of theAPC gene may play an important role in the genesis of certain breast carcinomas, and that another tumor-suppressor gene, which is the true target of frequent loss of heterozygosity, may exist near theAPC gene.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

LOH:

loss of heterozygosity

PCR:

polymerase chain reaction

RFLP:

restriction-fragment-length polymorphism

SSCP:

single-strand-conformation polymorphism

References

  • Ali IU, Lidereau R, Theillet C, Callahan R (1987) Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia. Science 238:185–188.

    PubMed  Google Scholar 

  • Baker SJ, Preisinger AC, Jessup JM, Paraskeva C, Markwitz S, Willson JKV, Hamilton S, Vogelstein B (1990) p53 gene mutations occur in combination with 17p allelic deletions as late events in colorectal tumorigenesis. Cancer Res 50:7717–7722

    PubMed  Google Scholar 

  • Bieche I, Champeme M-H, Matifas F, Cropp CS, Callahan R, Lidereau R (1993) Two distinct regions involved in 1p deletion in human primary breast cancer. Cancer Res 53:1990–1994

    PubMed  Google Scholar 

  • Borg A, Zhang Q-X, Alm P, Olsson H, Sellberg G (1992) The retinoblastoma gene in breast cancer: allele loss is not correlated with loss of gene protein expression. Cancer Res 52:2991–2994

    PubMed  Google Scholar 

  • Borresen A-L, Hoving E, Smith-Sorensen B, Malkin D, Lystad S, Andersen TI, Nesland JM, Isselbacher KJ, Friend SH (1991) Constant denaturant gel electrophoresis as a rapid screening technique for p53 mutations. Proc Natl Acad Sci USA 88:8405–8409

    PubMed  Google Scholar 

  • Boynton RF, Blount PL, Yin J, Brown VL, Huang Y, Tong Y, Tong Y, McDaniel T, Newkirk C, Resau JH, Raskind WH, Haggitt RC, Reid BJ, Meltzer SJ (1992) Loss of heterozygosity involving theAPC andMCC genetic loci occurs in the majority of human esophageal cancers. Proc Natl Acad Sci USA 89:3385–3388

    PubMed  Google Scholar 

  • Chen L-C, Dollbaum C, Smith HS (1989) Loss of heterozygosity on chromosome 1q in human breast cancer. Proc Natl Acad Sci USA 86:7204–7207

    PubMed  Google Scholar 

  • Chen L-C, Neubauer A, Kurisu W, Waldman FM, Ljung B-M, Goodson W III, Goldman ES, Moore D II, Balazs M, Liu E, Mayall BH, Smith HS (1991) Loss of heterozygosity on the short arm of chromosome 17 is associated with high proliferative capacity and DNA aneuploidy in human breast cancer. Proc Natl Acad Sci USA 88:3847–3851

    PubMed  Google Scholar 

  • D'Amico D, Carbone DP, Johnson BE, Meltzer SJ, Minna JD (1992) Polymorphic sites within theMCC andAPC loci reveal very frequent loss of heterozygosity in human small cell lung cancer. Cancer Res 52:1996–1999

    PubMed  Google Scholar 

  • Ding S-F, Habib NA, Dooley J, Wood C, Bowles L Delhanty JDA (1991) Loss of constitutional heterozygosity on chromosome 5q in hepatocellular carcinoma without cirrhosis. Br J Cancer 64:1083–1087

    PubMed  Google Scholar 

  • Fujimori M, Tokino T, Hino O, Kitagawa T, Imamura T, Okamoto E, Mitsunobu M, Ishikawa T, Nakagawa H, Harada H, Yagura M, Matssubara K, Nakamura Y (1991) Allelotype study of primary hepatocellular carcinoma. Cancer Res 51:89–93

    PubMed  Google Scholar 

  • Greewald BD, Harpaz N, Yin J, Huang Y, Tong Y, Brown VL, McDaniel T, Newkirk C, Resau JH, Meltzer SJ (1992) Loss of heterozygosity affecting thep53, Rb andmcc/apc tumor suppressor gene loci in dysplastic and cancerous ulcerative colitis. Cancer Res 52:741–745

    PubMed  Google Scholar 

  • Groden J, Thliveris A, Samowitz W, Carlson M, Gelbert L, Albertsen H, Joslyn G, Stevens J, Spirio L, Robertson M, Sargeant L, Krapcho K, Wolff E, Burt R, Hughes JP, Warrington J, McPherson J, Wasmuth J, Le Paslier D, Abderrahim H, Cohen D, Leppert M, White R (1991) Identification and characterization of the familial adenomatous polyposis coli gene. Cell 66:589–600

    PubMed  Google Scholar 

  • Horii A, Nakatsuru S, Miyoshi Y, Ichii S, Nagase H, Ando H, Yanagisawa A, Tsuchiya E, Kato Y, Nakamura Y (1992a) Frequent somatic mutations of theAPC gene in human pancreatic cancer. Cancer Res 52:6696–6698

    PubMed  Google Scholar 

  • Horii A, Nakatsuru S, Miyoshi Y, Ichii S, Nagase H, Kato Y, Yanagisawa A, Nakamura Y (1992b) TheAPC gene, responsible for familial adenomatous polyposis, is mutated in human gastric cancer. Cancer Res 52:3231–3233

    PubMed  Google Scholar 

  • Joslyn G, Carlson M, Thliveris A, Albertsen H, Gelbert L, Samowitz W, Groden J, Stevens J, Spirio L, Robertson M, Sargeant L, Krapcho K, Wolff E, Burt R, Hughes JP, Warrington J, McPherson J, Wasmuth J, Lepaslier D, Abderrahim H, Cohen D, Leppert M, White R (1991) Identification of deletion mutations and three new genes at the familial polyposis locus. Cell 66:601–613

    PubMed  Google Scholar 

  • Kinzler K, Nilbert MC, Su L-K, Vogelstein B, Byyan TM, Levy DB, Smith KJ, Preisinger AC, Hedge P, McKechnie D, Finniear R, Markham A, Groffen J, Miyoshi Y, Miki Y, Nishisho I, Nakamura Y (1991) Identification of FAP locus genes from chromosome 5q21. Science 253:661–665

    PubMed  Google Scholar 

  • Knudson AG JR (1971) Mutation and cancer: statistical study of retinoblastoma. Proc Natl Acad Sci USA 68:820–823

    PubMed  Google Scholar 

  • Lundberg C, Skoog L, Cavenee WK, Nordenskjold M (1987) Loss of heterozygosity in human ductal tumors indicates a recessive mutation on chromosome 13. Proc Natl Acad Sci USA 84:2372–2376

    PubMed  Google Scholar 

  • Mackay J, Steel CM, Elder PA, Forrest APM, Evans HJ (1988a) Allele loss on short arm of chromosome 17 in breast cancers. Lancet II:1384–1385

    Google Scholar 

  • Mackay J, Elder PA, Porteous DJ, Steel CM, Hawkins RA, Going JJ, Chetty U (1988b) Partial deletion of chromosome 11p in breast cancer correlates with size of primary tumor and oestrogen receptor level. Br J Cancer 58:710–714

    PubMed  Google Scholar 

  • Miyoshi Y, Ando H, Nagase H, Nishisho I, Horii A, Miki Y, Mori T, Utsunomiya J, Baba S, Peterson G, Hamilton SR, Kinzler KW, Vogelstein B, Nakamura Y (1992a) Germline-mutations of theAPC gene in 53 familial adenomatous polyposis patients. Proc Natl Acad Sci USA 89:4452–4456

    PubMed  Google Scholar 

  • Miyoshi Y, Nagase H, Ando H, Horii A, Ichii S, Nakatsuru S, Aoki T, Miki Y, Mori T, Nakamura Y (1992b) Somatic mutations of theAPC gene in colorectal tumors: mutation cluster region in theAPC gene. Hum Mol Genet 1:229–233

    PubMed  Google Scholar 

  • Morita R, Saito S, Ishikawa J, Ogawa O, Yoshida O, Yamakawa K, Nakamura Y (1991) Common regions of deletion on chromosome 5q, 6q, and 10q in renal cell carcinoma. Cancer Res 51:5817–5820

    PubMed  Google Scholar 

  • Nigro JM, Baker SJ, Preisinger AC, Jessup JM, Hostetter R, Cleary K, Bigner SH, Davidson N, Baylin S, Devilee P, Glover T, Collins FS, Weston A, Modili R, Harris CC, Vogelstein B (1989) Mutations in the p53 gene occur in diverse human tumor types. Nature 343:705–708

    Google Scholar 

  • Nishisho I, Nakamura Y, Miyoshi Y, Miki Y, Ando H, Horii A, Koyama K, Utsunomiya J, Baba S, Hedge P, Markham A, Krush AJ, Petersen G, Hamilton SR, Nirbert MC, Levy DB, Bryan TM, Preisinger AC, Smith KJ, Su L-K, Kinzler KW, Vogelstein B (1991) Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. Science 253:665–669

    PubMed  Google Scholar 

  • Ogasawara S, Maesawa C, Tamura G, Satodate R (1994) Lack of mutations of the adenomatous polyposis coli gene in oesophageal and gastric carcinomas. Virchows Arch 424:607–611

    PubMed  Google Scholar 

  • Osborne RJ, Merlo GR, Mitsudomi T, Venesio T, Liscia DS, Cappa APM, Chiba I, Takahashi T, Nau MM, Callahan R, Minna JD (1991) Mutations in the p53 gene in primary breast cancers. Cancer Res 51:6194–6198

    PubMed  Google Scholar 

  • Powell SM, Zilz N, Beazer-Barclay Y, Bryan TM, Hamilton SR, Thibodeau SN, Vogelstein B, Kinzler KW (1992)APC mutations occur early during colorectal tumorigenesis. Nature 359:235–237

    PubMed  Google Scholar 

  • Sano T, Tsujono T, Yoshida K, Nakayama H, Haruma K, Ito H, Nakamura Y, Kajiyama G, Tahara E (1991) Frequent loss of heterozygosity on chromosomes 1q, 5q, and 17p in human gastric carcinomas. Cancer Res 51:2926–2931

    PubMed  Google Scholar 

  • Sato T, Tanigami A, Yamakawa K, Akiyama F, Kasumi F, Sakamoto G, Nakamura Y (1990) Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer. Cancer Res 50:7184–7189

    PubMed  Google Scholar 

  • Sato T, Akiyama F, Sakamoto G, Kasumi F, Nakamura Y (1991) Accumulation of genetic alterations and progression of primary breast cancer. Cancer Res 51:5794–5799

    PubMed  Google Scholar 

  • Su L-K, Johnson KA, Smith KJ, Hill DE, Vogelstein B, Kinzler KW (1993) Association between wild type and mutantAPC gene products. Cancer Res 53:2728–2731

    PubMed  Google Scholar 

  • Suzuki Y, Sekiya T, Hayashi K (1991) Allele-specific polymerase chain reaction: a method for amplification and sequence determination of a single component among a mixture of sequence variants. Anal Biochem 192:82–84

    PubMed  Google Scholar 

  • Takita K, Sato T, Miyagi M, Watatani M, Akiyama F, Sakamoto G, Kasumi F, Abe R, Nakamura Y (1992) Correlation of loss of alleles on the short arms of chromosomes 11 and 17 with metastasis of primary breast cancer to lymph nodes. Cancer Res 52: 3914–3917

    PubMed  Google Scholar 

  • Tamura G, Kihara T, Nomura K, Terada M, Sugimura T, Hirohashi S (1991) Detection of frequent p53 gene mutations in primary gastric cancer by cell sorting and polymerase chain reaction singlestrand conformation polymorphism analysis. Cancer Res 51:3056–3058

    PubMed  Google Scholar 

  • Tamura G, Maesawa C, Suzuki Y, Ogasawara S, Terashima M, Saito K, Satodate R (1993) Primary gastric carcinoma cells frequetly lose heterozygosity at the APC and MCC genetic loci. Jpn J Cancer Res 84:1015–1018

    PubMed  Google Scholar 

  • Theillet C, Lidereau R, Escot C, Hutzell P, Brunet M, Gest J, Schlom J, Callahan R (1986) Loss of a c-H-ras-1 allele and aggressive human primary breast carcinomas. Cancer Res 46:4776–4781

    PubMed  Google Scholar 

  • Thompson AM, Morris RG, Wallace M, Wyllie AH, Steel CM, Carter DC (1993) Allele loss from 5q21 (APC/MCC) and 18q21 (DCC) and DCC mRNA expression in breast cancer. Br J Cancer 68:64–68

    PubMed  Google Scholar 

  • Tsuchiya E, Nakamura Y, Weng S-Y, Nakagawa K, Tsuchiya S, Sugano H, Kitagawa T (1992) Allelotype of non-small cell lung carcinoma — comparison between loss of heterozygosity in squamous cell carcinoma and adenocarcinoma. Cancer Res 52:2478–2481

    PubMed  Google Scholar 

  • Varesco L, Gismondi V, James R, Robertson M, Grammatico P, Groden J, Casarino L, De Benedetti L, Bafico A, Bertario L, Sala P, Sassatelli R, Ponz de Leon M, Biasco G, Allegretti A, Aste H, De Sanctis S Rossetti C, Illeni MT, Sciarra A, Del Porto G, White R, Ferrara GB (1993) Identification ofAPC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysis. Am J Hum Genet 52:280–285

    PubMed  Google Scholar 

  • Varley JM, Brammar WJ, Lane DP, Swallow JE, Dolan C, Walker RA (1991) Loss of chromosome 17p13 sequences and mutation of p53 in human breast carcinomas. Oncogene 6:413–421

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kashiwaba, M., Tamura, G. & Ishida, M. Aberrations of theAPC gene in primary breast carcinoma. J Cancer Res Clin Oncol 120, 727–731 (1994). https://doi.org/10.1007/BF01194271

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01194271

Key words

Navigation