PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2004 | 51 | 3 |

Tytuł artykułu

Detection of circulating breast cancer cells in peripheral blood by a two-marker reverse transcriptase-polymerase chain reaction assay

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The aim of this study was to use a two-marker assay for the detection of breast can­cer cells circulating in patients' blood. We have applied a PCR-based methodology to follow up the possibility of the development of metastatic disease in stage I and II pa­tients who had undergone curative surgery. Since the number of circulating cancer cells in peripheral blood is very low, the technique for their detection needs to be not only highly sensitive, but also very specific. The reverse transcriptase-polymerase chain reaction (RT-PCR) technique may improve the sensitivity of breast cancer cell detection up to only a few cells per one million. The principle of the RT-PCR assay is to amplify a messenger RNA characteristic for breast epithelial cells in a blood sam­ple. Since we do not expect such cells to be circulating in peripheral blood of healthy subjects, detection of the characteristic mRNA should indicate the presence of circu­lating breast cancer cells. We analyzed the usefulness of three mRNA markers: cytokeratin 19 (CK19), mammaglobin (hMAM) and S subunit of human chorionic gonadotropin (S-hCG) for this test. Blood samples (112) were obtained from 55 patients, in stages I and II, with or without metastasis to regional lymph nodes (N0 or N1). We found that a two-marker assay increases the sensitivity of detection of breast cancer cells in com­parison with a single-marker one. Combination of two tumor-specific mRNA mark­ers, hMAM/CK19 or S-hCG/CK19, allowed the detection of circulating breast cancer cells in 65% of N1 patients and 38% of N0 patients. By comparison, the combination hMAM/-hCG allowed the detection of circulating breast cancer cells in the blood of 68% of N1 patients and 46% of N0 patients. Addition of the third marker did not significantly increase the detection sensitivity.

Wydawca

-

Rocznik

Tom

51

Numer

3

Opis fizyczny

p.747-755,fig.,ref.

Twórcy

  • Cancer Center-Institute, W.Roentgena 5, 02-781 Warsaw, Poland
autor
autor

Bibliografia

  • Bilchik A, Miyashiro M, Kelley M, Kuo Ch, Fujiwara Y, Nakamori S, Monden M, Hoon DS. (2000) Molecular detection of metastatic pancreatic carcinoma cells using a multimarker reverse transcriptase-polymerase chain reaction assay. Cancer.; 88: 1037-44.
  • Bo M, Boime I. (1992) Identification of the transcriptionally active genes of the chorionic gonadotropin beta gene cluster in vivo. J Biol Chem.; 267: 3179-84.
  • Bostick PJ, Chatterjee S, Chi DD, Huynh KT, Giuliano AE, Cote R, Hoon DS. (1998) Limitations of specific reverse- transcriptase polymerase chain reaction markers in the detection of metastases in the lymph nodes and blood of breast cancer patients. J Clin Oncol.; 16: 2632-40.
  • Bostick PJ, Huynh KT, Sarantou T, Turner RR, Qi K, Giulliano AE, Hoon DS. (1998) Detection of metastasis in sentinel lymph nodes of breast cancer patients by multiple-marker RT-PCR. Int J Cancer.; 79: 645-51.
  • Brossart P, Keilholz U, Scheibenbogen C, Mohler T, Willhauck M, Hunstein W. (1994) Detection of residual tumor cells in patients with malignant melanoma responding to immunotherapy. J Immunother.; 15: 38-41.
  • Burchill SA, Bradbury MF, Pittman K, Southgate J, Smith B, Selby P. (1995) Detection of epithelial cancer cells in peripheral blood by reverse transcriptase-polymerase chain reaction. Br J Cancer. ; 71: 278-81.
  • Chomczynski P, Sacchi N. (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol- chloroform extraction. Anal Biochem.; 162: 156-9.
  • Datta YH, Adams PT, Drobyski WR, Ethier SP, Terry VH, Roth MS. (1994) Sensitive detection of occult breast cancer by the reverse- transcriptase polymerase chain reaction. J Clin Oncol.; 12: 475-82.
  • Didkowska J, Wojciechowska U, Tarkowski W, Zatonski W. (2002) Nowotworyzlosliwe wPolsce w 1999r. Centrum Onkologii, Warszawa (in Polish)..
  • Hautkappe AL, Lu M, Mueller H, Bex A, Harstrick A, Roggendorf M, Ruebben H. (2000) Detection of germ-cell tumor cells in the peripheral blood by nested reverse transcription-polymerase chain reaction for alpha-fetoprotein-messenger RNA and beta human chorionic gonadotropin-messenger RNA. Cancer Res.; 60: 3170-4.
  • Hildebrandt M, Mapara MY, Korner IJ, Bargou RC, Moldenhauer G, Dorken B. (1997) Reverse transcriptase-polymerase chain reaction (RT-PCR)-controlled immunomagnetic purging of breast cancer cells using the magnetic cell separation (MACS) system: a sensitive method for monitoring purging efficiency. Exp Hematol.; 25: 57-65.
  • Kruger W, Krzizanowski C, Holweg M, Stockschlader M, Kroger N, Jung R, Mross K, Jonat W, Zander AR. (1996) Reverse transcriptase/polymerase chain reaction detection of cytokeratin-19 mRNA in bone marrow and blood of breast cancer patients. J Cancer Res Clin Oncol.; 122: 679-86.
  • Kulik J, Nowecki ZI, Rutkowski P, Ruka W, Rochowska M, Skurzak H, Siedlecki JA. (2001) Detection of circulating melanoma cells in peripheral blood by a two-marker RT-PCR assay. Melanoma Res.; 11: 65-73.
  • Leitzel K, Lieu B, Curley E, Smith J, Chinchilli V, Rychlik W, Lipton A. (1998) Detection of cancer cells in peripheral blood of breast cancer patients using reverse transcription-polymerase chain reaction for epidermal growth factor receptor. Clin Cancer Res.; 4: 3037-43.
  • Madersbacher S, Kratzik C, Gerth R, Dirnhofer S, Berger P. (1994) Human chorionic gonadotropin (hCG) and its free subunits in hydrocele fluids and neoplastic tissue of testicular cancer patients: insights into the in vivo hCG-secretion pattern. Cancer Res.; 54: 5096-100.
  • Marcillac I, Troalen F, Bidart JM, Ghillani P, Ribrag V, Escudier B, Malassagne B, Droz JP, Lhomme C, Rougier P, et al. (1992) Free human chorionic gonadotropin beta subunit in gonadal and nongonadal neoplasms. Cancer Res.; 52: 3901-7.
  • McManus LM, Naughton MA, Martinez-Hernandez A. (1976) Human chorionic gonadotropin in human neoplastic cells. Cancer Res. ; 36: 3476-81.
  • Sarantou T, Chi DD, Garrison DA, Conrad AJ, Schmid P, Morton DL, Hoon DS. (1997) Melanoma-associated antigens as messenger RNA detection markers for melanoma. Cancer Res.; 57: 1371-6.
  • Schoenfeld A, Luqmani Y, Smith D, O'Reilly S, Shousha S, Sinnett HD, Coombes RC. (1994) Detection of breast cancer micrometastases in axillary lymph nodes by using polymerase chain reaction. Cancer Res.; 54: 2986-90.
  • Taback B, Chan AD, Kuo ChT, Bostick PJ, Wang HJ, Giuliano AE, Hoon DS. (2001) Detection of occult metastatic breast cancer cells in blood by a multimolecular marker assay: Correlation with clinical stage of disease. Cancer Res.; 61: 8845-50.
  • Vogelstein B, Kinzler KW. (1993) The multistep nature of cancer. Trends Genet.; 9: 138-41.
  • Watson MA, Dintzis S, Darrow CM, Voss LE, DiPersio J, Jensen R, Fleming TP. (1999) Mammaglobin expression in primary, metastatic, and occult breast cancer. Cancer Res.; 59: 3028-31.
  • Watson MA, Fleming TP. (1996) Mammaglobin, a mammary-specific member of the uteroglobin gene family, is overexpressed in human breast cancer. Cancer Res.; 56: 860-5.
  • Zach O, Kasparu H, Krieger O, Hehenwarter W, Girschikofsky M, Lutz D. (1999) Detection of circulating mammary carcinoma cells in the peripheral blood of breast cancer patients via a nested reverse transcriptase polymerase chain reaction assay for mammaglobin mRNA. J Clin Oncol.; 17: 2015-9.
  • Zippelius A, Pantel K. (2000) RT-PCR-based detection of occult disseminated tumor cells in peripheral blood and bone marrow of patients with solid tumors. Ann NY Acad Sci.; 906: 110-23.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-c528b8af-2c43-4bfe-8fec-35a237a650b7
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.