2
Views
0
CrossRef citations to date
0
Altmetric
Articles

Molecular Biology Techniques in Malignant Lymphoma

Pages 213-218 | Published online: 18 Jul 2013

References

  • Southern E: Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98:503–517, 1975
  • Saiki RK, Gelfand DH, Stoffel S et al: Primer-directed enzymatic amplification of DNA with thermostable DNA polymerase. Science 239:487–491, 1988
  • Kwok S, Higuchi R: Avoiding false positives with PCR. Nature 339:237–238, 1989
  • Yunis JJ, Oken MM, Kaplan ME et al. Distinctive chromosomal abnormalities in histologic sub-types of Non-Hodgkin's lymphomas. N Engl J Med 307:1231–1236, 1982
  • Cotter F, Price C, Zucca E, Young D: Direct sequence analysis of the 14q+ and 18q— chromosome junctions in follicular lymphoma. Blood 76:131–135, 1990
  • Croce CM, Nowell PC: Molecular basis of human B cell neoplasia. Blood 65:1–7, 1985
  • Bakhshi A, Wright JJ, Groninger W et al: Mechanism of the t(14;18) chromosomal translocation. Structural analysis of both derivative 14 and 18 reciprocal partners. Proc Natl Acad Sci USA 84:2396–2400, 1987
  • Limpens J, de Jong D, Voetdjik AMH et al: Translocation t(14;18) in benign B-lymphocytes. Blood 76: 237a, 1990 (abstr suppl 1)
  • Nowell PC, Croce CM: Chromosomal approaches to oncogenes and oncogenesis. FASEB J 2:3054–3060, 1988
  • Strasser A, Harris AW, Bath ML, Cory S: Novel primitive lymphoid tumours induced in transgenic mice by cooperation between myc and bc1-2. Nature 348:331–333, 1990
  • Aisenberg AC, Wilkes BM, Jacobson JO: The bc1-2 gene is rearranged in many diffuse B-cell lymphomas. Blood 71:969–972, 1988
  • Lee M-S, Blick MB, Pathak S et al: The gene located at chromosome 18 band q21 is rearranged in uncultured diffuse lymphomas as well as follicular lymphomas. Blood 70:90–95, 1987
  • Cleary ML, Chao J, Warnke R, Sklar J: Immunoglobulin gene rearrangement as a diagnostic criterion of B-cell lymphoma. Proc Nati Acad Sci USA 81:593–587, 1984
  • Ngan BY, Nourse J, Cleary ML: Detection of chromosomal translocation t(14 ;18) within the minor cluster region of bc1-2 by polymerase chain reaction and direct genomic sequencing of the enzymatically amplified DNA in follicular lymphomas. Blood 73:1759–1762, 1987
  • Weiss LM, Warnke RA, SIdar J, Cleary ML: Molecular analysis of the t(14;18) chromosomal translocation in malignant lymphomas. New Engl J Med 317:1185–1189, 1987
  • Tsujimoto Y, Bashir MM, Givol J et al: DNA rearrangements in human follicular lymphoma can involve the 5' or the 3' region of the bc1-2 gene. Proc Natl Acad Sci USA 84:1329–1331, 1987
  • Pezzella F, Ralfkaien E, Gatter KC, Masons DY: The 14;18 translocation in European cases of follicular lymphoma: Comparison of Southern blotting and the polymerase chain reaction. Br J Haematol 76:58–64, 1990
  • Pezella F, Gatter KC, Mason DY: Detection of 14;18 chromosomal translocation in paraffin embedded lymphoma tissue. Lancet April 8: 779–780, 1989
  • Crescenzi M, Seto M, Herzig GP et al: Thermostable DNA polymerase chain amplification of t(14 ;18) chromosome break-points and detection of minimal residual disease. Proc Natl Acad Sci USA 85:4869–4873, 1988
  • Stetler-Stevenson M, Crush-Statton S., Cossman J: Involvement of the bc1-2 gene in Hodgkin's disease. J Natl Canc Inst 82:855–858, 1990
  • Louie DC, Kant JA, Brooks JJ, Reed JC: Absence of t(14;18) major and minor breakpoints and of Bc1-2 protein overproduction in Reed-Sternberg cells of Hodgkin's disease. Am J Pathol 139:1231–1237, 1991
  • Nishikura K, ar-Rushdi A, Erikson J et al: Differential expres-sion of the normal and of the translocated human c-myc oncogene in B cells. Proc Natl Acad Sci USA 80:4822–4826, 1983
  • Dalla-Favera R, Bregni M, Erikson J et al: Assignment of the human c-myc oncogene to the region of chromosome 8 which is translocated in Burkitt's lymphoma cells. Proc Natl Acad Sci USA 79:7824–7825, 1982
  • Dalla-Favera R, Martinotti S, Gallo RC et al: Translocation and rearrangements of the c-myc oncogene in human differentiated B-cell lymphomas. Science 219:963–967, 1983
  • Adams JM, Gerondialcis S, Webb E et al: Cellular myc oncogene is altered by chromosome translocation to an immunoglobulin locus in murine plasmacytomas and is rearranged similarly in Burkitt lymphomas. Proc Natl Acad Sci USA 80: 1982–1986, 1983
  • Nishilcura K, ar-Rushdi A, Erikson J et al: Re-expression of rearranged 4 gene and translocated c-myc in mouse 313 cells x Burkitt lymphoma cell hybrids. Science 224:399–402, 1984
  • Shiramizu B, Magrath I: Localisation of break-points by polymerase chain reactions in Burkitt's lymphoma with 8;14 translocations. Blood 75:1848–1852, 1990
  • Tsujimoto Y, Yunis J, Onorato-Showe L et al: Molecular cloning of the chromosomal break-point of B-cell lymphomas and leukaemias with the t(11;14) chromosomal translocation. Science 224:1403–1406, 1984
  • Tsujimoto Y, Jaffe E, Cossman J et al: Clustering of break-points on chromosome 11 in human B cell neoplasms with the t(11;14) chromosome translocation. Nature 315:340–343, 1985
  • Medeiros LJ, van Krieken JH, Jaffe ES, Raffeld M: Association of bc1-1 rearrangement with lymphocytic lymphoma of intermediate differentiation. Blood 76:2086–2090, 1990
  • Williams ME, Westerman CD, Swerdlow SH: Genotypic characterisation of centrocytic lymphoma: Frequent rearrangement of the chromosome 11 bc1-1 locus. Blood 76:1387–1391, 1990
  • Nishida K, Taniwalci M, Misawa S, Abe T: Non-random rear-rangement of chromosome 14 at band q32.33 in human lym-phoid malignancies with mature B-cell phenotype. Cancer Res 49:1275–1281, 1989
  • Barriga F, Kiwanuka J, Alvarez-Mon M et al: Significance of chromosome 8 breakpoint location in Burkitt's lymphoma; Correlation with geographical origin and association with Epstein-Barr virus. Current Top Microbiol Immunol 141:128–137, 1988
  • Saito I, Servenius B, Compton T, Fox RI: Detection of Ep-stein-Barr virus DNA by polymerase chain reaction in blood and tissue biopsies from patients with Sjogren's syndrome. J Exp Med 169:2191–2198, 1989
  • Okano B, Bashir RM, Davis JR, Purtilo DT: Detection of primary Epstein-Barr virus infection in a patient with X-linked lymphoproliferative disease receiving immunoglobulin prophylaxis. Am J Hem 36;294–296, 1991
  • Tonegawa S: Somatic generation of antibody diversity. Nature 302:575–581, 1983
  • Korsmeyer SJ, Arnold A, Balchshi A, Ravetch JV et al: Immunoglobulin gene rearrangement and cell surface antigen expression in acute lymphocytic leukaemias of T cell and B cell precursor origins. J Clin Invest 71:301–313, 1983
  • Tawa A, Hozumi N, Minden M et al: Rearrangement of the T-cell receptor 3 chain gene in non-T-cell and non-B-cell acute lymphoblastic leukaemia of childhood. New Engl J Med 313: 1033–1037, 1985
  • Flug F, Pellici PG, Bonetti F et al: T-cell receptor gene rear-rangements as markers of lineage and clonality in T-cell neo-plasms. Proc Nati Acad Sci USA 82:3460–3464, 1985
  • Ha K, Hozumi M, Hrincu A, Gelfand EW: Lineage specific classification of leukaemia: the analysis of 60 cases of child-hood leukaemia. Br J Haematol 61:237–249, 1985
  • Story CJ, Turner DR, Morley AA, Seshadri R: Diagnostic use of immunoglobulin and T-cell receptor gene rearrangements in lymphoproliferative disease. Aust N Z J Med 17:1–8, 1987
  • MacIntyre EA, Sigaux F: T cell receptorCurrent state ofknowledge and potential clinical application in haematology. Br J Haematol 72:28–31, 1989
  • McCarthy KP, Sloane JP, Wiedemann LM: Rapid method for distinguishing clonal from polyclonal B cell populations in sur-gical biopsy specimens. J Clin Pathol 43:429–432, 1990
  • McCarthy KP, Sloane JP, Kabarowski JH et al: The rapid de-tection of clonal T-cell proliferation in patients with lymphoid disorders. Am J Pathol 138:821–828, 1991
  • Brisco MJ, Tan L-W, Orsborn AM, Morley AA: Development of a highly sensitive assay, based on the polymerase chain reac-tion, for rare B-Iymphocytic clones in a polyclonal population. Br J Haematol 75:163–167, 1990
  • Trainor KT, Brisco MJ, Story CJ, Morley AA: Monoclonality in B-lymphoproliferative disorders detected at the DNA level. Blood 75:2220–2222, 1990
  • Trainor KJ, Brisco MJ, Wan JH et al: Gene rearrangement in B- and T-lymphoproliferative disease detected by the polymer-ase chain reaction. Blood 78:192–196, 1991
  • Bourguin A, Tung R, Galili N, Sklar J: Rapid nonradioactive detection of clonal T-cell receptor gene rearrangements in lym-phoid neoplasms. Proc Natl Acad Sci USA 87:8536–8540, 1990
  • Deane M, Norton JD: Immunoglobulin gene "fingerprinting": an approach to analysis of B lymphoid clonality in lym-phoproliferative disorders. Br J Haematol 77:274–281, 1991
  • Bates I, Bedu-Addo G, Bevan DH, Rutherford TR: Use of im-munoglobulin gene rearrangements to show clonal lym-phoproliferation in hyper-reactive malarial splenomegaly. Lan-cet 337:505–507, 1991
  • Wan JH, Trainor KJ, Brisco MJ, Morley AA: Monoclonality in B cell lymphoma detected in paraffin embedded sections by use of the polymerase chain reaction. J Clin Pathol 43:888–890, 1990
  • Wan JH, Sykes PJ, Orell SR, Morley AA: A rapid method for the detection of monoclonality in B-cell lymphoma in lymph node aspirates using the polymerase chain reaction. J Clin Pathol 45:420–423, 1992
  • Fey MF, Kulozik AE, Hansen-Hagge TE, Tobler A: The poly-merase chain reaction: A new tool for the detection of minimal residual disease in haematological malignancies. Eur J Cancer 2789–2794, 1991
  • Hansen-Hagge TE, Yokota S, Bartram CR: Detection of mini-mal residual disease in acute lymphoblastic leukaemia by in vitro amplification of rearranged T-cell receptor chain se-quence. Blood 74:1762–167, 1989
  • Yamada M, Hudson S, Tournay O et al: Detection of minimal disease in hematopoietic malignancies of the B-cell lineage by using third-complementarity-determining region (CDR-III)-specific probes. Proc Natl Acad Sci USA 86:5123–5127, 1989
  • Yamada M, Wasserman R, Lange B et al: Minimal residual dis-ease in childhood B-lineage lymphoblastic leukaemia. New Engl J Med 323:448–455, 1990
  • Brisco MJ, Condon J, Sykes PJ et al: Detection and quantita-tion of neoplastic cells in acute lymphoblastic leukaemia, by the use of the polymerase chain reaction. Br J Haematol 79: 211–217, 1991
  • Stetler-Stevenson M, Raffeld M, Cohen P, Cossman J: Detec-tion of occult follicular lymphoma by specific DNA amplifica-tion. Blood 72:1822–1825, 1988
  • Lee M-S, Chang K-S, Cabanillas F et al: Detection of minimal residual cells carrying the t(14;18) by DNA sequence am-plification. Science 237:175–178, 1987
  • Gribben JG, Freedman AS, Woo SD et al: All advanced stage non-Hodgkin's lymphomas with a polymerase chain reaction amplifiable breakpoint of bc1-2 have residual cells containing the bc1-2 rearrangement at evaluation and after treatment. Blood 78:3275–3280, 1991
  • Sykes PJ, Neoh SH, Brisco MJ et al: Quantitation for targets for the polymerase chain reaction by use of limiting dilution. Biotechniques (in press), 1992
  • Mercier B, Gaucher C, Feugeas O, Mazurier C: Direct PCR of whole blood, without DNA extraction. Nucleic Acids Res 18:5908, 1990
  • McHale RH, Stapleton PM, Berquist PL: Rapid preparation of blood and tissue samples for polymerase chain reaction. Biotechniques 10:20–22, 1991
  • Beutler E, Gelbart T, Kuhl W: Interference of heparin with the polymerase chain reaction. Biotechniques 9:166, 1990

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.