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MGEA6 is tumor-specific overexpressed and frequently recognized by patient-serum antibodies

Abstract

Tumorigenesis of meningioma has been associated with chromosome 22, most notably the NF2 gene, but additional genes have also been implicated in meningioma development. Previously, we have cloned the cDNAs for the meningioma expressed antigen 6 (MGEA6) and its splice variant MGEA11. Here, we show that antibodies against recombinantly expressed MGEA6/11 are found in 41.7% (10/24) of the sera from meningioma patients and in 2/8 sera of glioblastoma patients, whereas no response was seen in 12 sera from healthy persons. Western-blot analyses using generated polyclonal antibodies, revealed overexpression in meningioma and glioma tumor samples compared to normal brain. Immunohistochemical staining of tissue sections confirms reactivity in meningioma tumor cells and tumor cells of glial origin. We found no reactivity to normal astrocytes and only faint reactivity to normal leptomeninges. Sequence analysis predicted membranic localization of MGEA6/11, that was confirmed by cell fractionation. The immune response to MGEA6/11 is frequent in both meningioma and glioma patients and may likely be attributed to overexpression of the MGEA6/11 protein in the tumor cells.

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References

  • Akagi K, Kurahashi H, Arita N, Hayakawa T, Monden M, Mori T, Takai S, Nishisho I . 1995 Int. J. Cancer 60: 178–182

  • Barker CF, Billingham RE . 1977 Adv. Immunol. 25: 1–54

  • Becker I, Roggendorf W . 1989 J. Neuroimmunol. 25: 161–167

  • Ben-Mahrez K, Sorokine I, Thierry D, Kawasumi T, Ishi S, Salmon R, Kohiyama M . 1990 Int. J. Cancer 46: 35–38

  • Boon T, Lloyd JO . 1997 Curr. Opin. Immunol. 9: 681–683

  • Comtesse N, Heckel D, Racz A, Brass N, Glass B, Meese E . 1999 Clin. Cancer Res. 5: 3560–3568

  • Comtesse N, Reus K, Meese E . 2001 Genomics 75: 43–48

  • Disis ML, Cheever MA . 1996 Curr. Opin. Immunol. 8: 637–642

  • Disis ML, Calenoff E, McLaughlin G, Murphy AE, Cehn W, Groner B, Jeschke B, Lydon N, McGlynn E, Livingston RB, Moe R, Cheever MA . 1994 Cancer Res. 54: 16–20

  • Gallagher G, Al-Azzawi F, Walsh LP, Wilson G, Handley J . 1991 Br. J. Cancer 61: 35–40

  • Harlow E, Lane D . 1988 Antibodies A Laboratory Manual Cold Spring Harbor Laboratory: USA

    Google Scholar 

  • Heckel D, Brass N, Fischer U, Blin N, Steudel I, Türeci Ö, Fackler O, Zang KD, Meese E . 1997 Hum. Mol. Genet. 6: 2031–2041

  • Heckel D, Comtesse N, Brass N, Blin N, Zang D, Meese E . 1998 Hum. Mol. Genet. 7: 1859–1872

  • Kleihues P, Cavenee WK . 2000 Pathology & Genetics. Tumours of the Nervous System IARC Press: France

    Google Scholar 

  • Marcias MJ, Hyvonen M, Baraldi E, Schultz J, Sudol M, Saraste M, Oschkinat H . 1996 Nature 382: 646–649

  • Merrifield RB . 1963 J. Am. Chem. Soc. 85: 2149–2158

  • Pees HW, Seidel B . 1976 Clin. Exp. Immunol. 24: 310–316

  • Pees HW . 1979 Acta. Neurochir. (Wien) 50: 217–227

  • Pupa SM, Menard S, Andreola S, Colnaghi MI . 1996 Cancer Res. 53: 5864–

  • Real FX, Furukaw KS, Mattes MJ, Gusik SA, Cordon-Cardo C, Oettgen HF, Old LJ, Lloyd KO . 1988 Proc. Natl. Acad. Sci. USA 85: 3965–3969

  • Ruttledge MH, Sarrazin J, Rangaratnam S, Phelan CM, Twist E, Merel P, Delattre O, Thomas G, Nordenskjold M, Collins VP, Dumanski JP, Rouleau GA . 1994 Nature Genet. 6: 180–184

  • Tabuchi K, Kawakami Y, Nishimoto A . 1979 Acta. Neurochi. (Wien) 55: 201–211

  • Yamamoto A, Shimiziu E, Ogura T, Sone S . 1996 Int. J. Cancer 69: 283–289

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Acknowledgements

The authors thank Prof Dr WI Steudel and the staff of the Neurosurgical Clinic for providing fresh tumor samples. We thank Mr Marc Voss, Department of Virology, for the excellent help preparing the cell fractions. The skilled technical assistance of Mr W Förderer, Mr P Krück, Mrs S Leyes, Mrs B Simon and Mr B Stock, Department of Neuropathology, is greatly appreciated. This work was supported by a grant from the Deutsche Forschungsgemeinschaft (SFB 399, A4).

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Correspondence to Eckart Meese.

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Comtesse, N., Niedermayer, I., Glass, B. et al. MGEA6 is tumor-specific overexpressed and frequently recognized by patient-serum antibodies. Oncogene 21, 239–247 (2002). https://doi.org/10.1038/sj.onc.1205005

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