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Construction of an immunotoxin, D2C7-(scdsFv)-PE38KDEL, targeting EGFRwt and EGFRvIII for brain tumor therapy.

Publication ,  Journal Article
Chandramohan, V; Bao, X; Keir, ST; Pegram, CN; Szafranski, SE; Piao, H; Wikstrand, CJ; McLendon, RE; Kuan, C-T; Pastan, IH; Bigner, DD
Published in: Clin Cancer Res
September 1, 2013

PURPOSE: The EGF receptor gene (EGFR) is most frequently amplified and overexpressed, along with its deletion mutant, EGFRvIII, in glioblastoma. We tested the preclinical efficacy of the recombinant immunotoxin, D2C7-(scdsFv)-PE38KDEL, which is reactive with a 55-amino acid (AA) region present in the extracellular domain of both EGFRwt (583-637 AAs) and EGFRvIII (292-346 AAs) proteins. EXPERIMENTAL DESIGN: The binding affinity and specificity of D2C7-(scdsFv)-PE38KDEL for EGFRwt and EGFRvIII were measured by surface-plasmon resonance and flow cytometry. In vitro cytotoxicity of D2C7-(scdsFv)-PE38KDEL was measured by inhibition of protein synthesis in human EGFRwt-transfected NR6 (NR6W), human EGFRvIII-transfected NR6 (NR6M), EGFRwt-overexpressing A431-epidermoid-carcinoma, and glioblastoma xenograft cells (43, D08-0493MG, D2159MG, and D270MG). In vivo antitumor efficacy of D2C7-(scdsFv)-PE38KDEL was evaluated using 43, NR6M, and D270MG orthotopic tumor models. RESULTS: The KD of D2C7-(scdsFv)-PE38KDEL for EGFRwt and EGFRvIII was 1.6×10(-9) mol/L and 1.3×10(-9) mol/L, respectively. Flow cytometry with NR6W and NR6M cells confirmed the specificity of D2C7-(scdsFv)-PE38KDEL for EGFRwt and EGFRvIII. The D2C7-(scdsFv)-PE38KDEL IC50 was 0.18 to 2.5 ng/mL on cells expressing EGFRwt (NR6W, A431, 43, and D08-0493MG). The D2C7-(scdsFv)-PE38KDEL IC50 was approximately 0.25 ng/mL on EGFRvIII-expressing cells (NR6M) and on EGFRwt- and EGFRvIII-expressing glioblastoma xenograft cells (D2159MG and D270MG). Significantly, in intracranial tumor models of 43, NR6M, and D270MG, treatment with D2C7-(scdsFv)-PE38KDEL by convection-enhanced delivery prolonged survival by 310% (P=0.006), 28% (P=0.002), and 166% (P=0.001), respectively. CONCLUSIONS: In preclinical studies, the D2C7-(scdsFv)-PE38KDEL immunotoxin exhibited significant potential for treating brain tumors expressing EGFRwt, EGFRvIII, or both.

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Published In

Clin Cancer Res

DOI

EISSN

1557-3265

Publication Date

September 1, 2013

Volume

19

Issue

17

Start / End Page

4717 / 4727

Location

United States

Related Subject Headings

  • Xenograft Model Antitumor Assays
  • Surface Plasmon Resonance
  • Oncology & Carcinogenesis
  • Immunotoxins
  • Immunoglobulin G
  • Humans
  • Glioblastoma
  • Flow Cytometry
  • ErbB Receptors
  • Epitopes
 

Citation

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Chandramohan, V., Bao, X., Keir, S. T., Pegram, C. N., Szafranski, S. E., Piao, H., … Bigner, D. D. (2013). Construction of an immunotoxin, D2C7-(scdsFv)-PE38KDEL, targeting EGFRwt and EGFRvIII for brain tumor therapy. Clin Cancer Res, 19(17), 4717–4727. https://doi.org/10.1158/1078-0432.CCR-12-3891
Chandramohan, Vidyalakshmi, Xuhui Bao, Stephen T. Keir, Charles N. Pegram, Scott E. Szafranski, Hailan Piao, Carol J. Wikstrand, et al. “Construction of an immunotoxin, D2C7-(scdsFv)-PE38KDEL, targeting EGFRwt and EGFRvIII for brain tumor therapy.Clin Cancer Res 19, no. 17 (September 1, 2013): 4717–27. https://doi.org/10.1158/1078-0432.CCR-12-3891.
Chandramohan V, Bao X, Keir ST, Pegram CN, Szafranski SE, Piao H, et al. Construction of an immunotoxin, D2C7-(scdsFv)-PE38KDEL, targeting EGFRwt and EGFRvIII for brain tumor therapy. Clin Cancer Res. 2013 Sep 1;19(17):4717–27.
Chandramohan, Vidyalakshmi, et al. “Construction of an immunotoxin, D2C7-(scdsFv)-PE38KDEL, targeting EGFRwt and EGFRvIII for brain tumor therapy.Clin Cancer Res, vol. 19, no. 17, Sept. 2013, pp. 4717–27. Pubmed, doi:10.1158/1078-0432.CCR-12-3891.
Chandramohan V, Bao X, Keir ST, Pegram CN, Szafranski SE, Piao H, Wikstrand CJ, McLendon RE, Kuan C-T, Pastan IH, Bigner DD. Construction of an immunotoxin, D2C7-(scdsFv)-PE38KDEL, targeting EGFRwt and EGFRvIII for brain tumor therapy. Clin Cancer Res. 2013 Sep 1;19(17):4717–4727.

Published In

Clin Cancer Res

DOI

EISSN

1557-3265

Publication Date

September 1, 2013

Volume

19

Issue

17

Start / End Page

4717 / 4727

Location

United States

Related Subject Headings

  • Xenograft Model Antitumor Assays
  • Surface Plasmon Resonance
  • Oncology & Carcinogenesis
  • Immunotoxins
  • Immunoglobulin G
  • Humans
  • Glioblastoma
  • Flow Cytometry
  • ErbB Receptors
  • Epitopes