Identification, characterization, and targeting of IL-4 receptor by IL-4-pseudomonas exotoxin in mouse models of anaplastic thyroid cancer

Bharat H. Joshi, Akiko Suzuki, Toshio Fujisawa, Pamela Leland, Frederick Varrichio, Samir Lababidi, Ricardo Lloyd, Jan Kasperbauer, Raj K. Puri

Research output: Contribution to journalArticle

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Abstract

Thyroid cancer is a rapidly increasing endocrine cancer. Since interleukin-4 receptor (IL-4R) is overexpressed in human solid cancer, we examined expression of IL-4R in 50 cases of anaplastic thyroid cancer (ATC), 37 well-differentiated papillary cancer (WDPC), 35 well-differentiated follicular cancer of thyroid (WDFC), and 37 normal thyroid specimens by immunohistochemistry (IHC) and in-situ hybridization (ISH) techniques. We demonstrated that IL-4Rα was overexpressed in 36/50 (72%) ATC, 20/35 (57%) WDFC, and 11/37 (30%) WDPC tumors. Other two subunits of IL-4R, interleukin-13 receptor α1 (IL-13Rα1) and interleukin-2 receptor gamma (IL-2RγC), were either weakly expressed or absent. As ATC is a highly aggressive cancer with higher incidence of IL-4Rα expression, we characterized IL-4R in 3 ATC cell lines. RT-qPCR and IFA results showed that IL-4Rα is overexpressed while IL-13Rα1 is weakly expressed. Control human umbilical vein endothelial cell line (HUVEC) showed weak expression of IL-4Rα. Binding and competition studies with 125I-IL-4 in ATC cell lines demonstrated that IL-4 specifically bound to IL-4Rα on cell surface. ATC cell lines were highly sensitive to a chimeric fusion cytotoxin consisting of circularly permuted IL-4 and truncated Pseudomonas exotoxin (IL-4-PE), which killed them in a concentration dependent manner. IL-4-PE also blocked colony formation of ATC cell lines in clonogenic assays. IL-4-PE mediated a significant antitumor activity in mouse models of ATC. Intratumoral administration of IL-4-PE caused significant regression of established tumors in a dose dependent manner and increased the overall survival without any visible toxicity. Thus, IL-4Rα in ATC may represent a novel therapeutic target and IL-4-PE may serve as an investigational therapeutic option for ATC.

Original languageEnglish (US)
Pages (from-to)273-284
Number of pages12
JournalDiscovery medicine
Volume20
Issue number111
StatePublished - Jan 1 2015

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Interleukin-4 Receptors
Exotoxins
Pseudomonas
Interleukin-4
Cell Line
Interleukin-13 Receptors
Neoplasms
Endocrine Gland Neoplasms
Anaplastic Thyroid Carcinoma
Interleukin-2 Receptors
Human Umbilical Vein Endothelial Cells
Cytotoxins
Thyroid Neoplasms
In Situ Hybridization
Thyroid Gland
Immunohistochemistry

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Joshi, B. H., Suzuki, A., Fujisawa, T., Leland, P., Varrichio, F., Lababidi, S., ... Puri, R. K. (2015). Identification, characterization, and targeting of IL-4 receptor by IL-4-pseudomonas exotoxin in mouse models of anaplastic thyroid cancer. Discovery medicine, 20(111), 273-284.

Identification, characterization, and targeting of IL-4 receptor by IL-4-pseudomonas exotoxin in mouse models of anaplastic thyroid cancer. / Joshi, Bharat H.; Suzuki, Akiko; Fujisawa, Toshio; Leland, Pamela; Varrichio, Frederick; Lababidi, Samir; Lloyd, Ricardo; Kasperbauer, Jan; Puri, Raj K.

In: Discovery medicine, Vol. 20, No. 111, 01.01.2015, p. 273-284.

Research output: Contribution to journalArticle

Joshi, BH, Suzuki, A, Fujisawa, T, Leland, P, Varrichio, F, Lababidi, S, Lloyd, R, Kasperbauer, J & Puri, RK 2015, 'Identification, characterization, and targeting of IL-4 receptor by IL-4-pseudomonas exotoxin in mouse models of anaplastic thyroid cancer', Discovery medicine, vol. 20, no. 111, pp. 273-284.
Joshi BH, Suzuki A, Fujisawa T, Leland P, Varrichio F, Lababidi S et al. Identification, characterization, and targeting of IL-4 receptor by IL-4-pseudomonas exotoxin in mouse models of anaplastic thyroid cancer. Discovery medicine. 2015 Jan 1;20(111):273-284.
Joshi, Bharat H. ; Suzuki, Akiko ; Fujisawa, Toshio ; Leland, Pamela ; Varrichio, Frederick ; Lababidi, Samir ; Lloyd, Ricardo ; Kasperbauer, Jan ; Puri, Raj K. / Identification, characterization, and targeting of IL-4 receptor by IL-4-pseudomonas exotoxin in mouse models of anaplastic thyroid cancer. In: Discovery medicine. 2015 ; Vol. 20, No. 111. pp. 273-284.
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abstract = "Thyroid cancer is a rapidly increasing endocrine cancer. Since interleukin-4 receptor (IL-4R) is overexpressed in human solid cancer, we examined expression of IL-4R in 50 cases of anaplastic thyroid cancer (ATC), 37 well-differentiated papillary cancer (WDPC), 35 well-differentiated follicular cancer of thyroid (WDFC), and 37 normal thyroid specimens by immunohistochemistry (IHC) and in-situ hybridization (ISH) techniques. We demonstrated that IL-4Rα was overexpressed in 36/50 (72{\%}) ATC, 20/35 (57{\%}) WDFC, and 11/37 (30{\%}) WDPC tumors. Other two subunits of IL-4R, interleukin-13 receptor α1 (IL-13Rα1) and interleukin-2 receptor gamma (IL-2RγC), were either weakly expressed or absent. As ATC is a highly aggressive cancer with higher incidence of IL-4Rα expression, we characterized IL-4R in 3 ATC cell lines. RT-qPCR and IFA results showed that IL-4Rα is overexpressed while IL-13Rα1 is weakly expressed. Control human umbilical vein endothelial cell line (HUVEC) showed weak expression of IL-4Rα. Binding and competition studies with 125I-IL-4 in ATC cell lines demonstrated that IL-4 specifically bound to IL-4Rα on cell surface. ATC cell lines were highly sensitive to a chimeric fusion cytotoxin consisting of circularly permuted IL-4 and truncated Pseudomonas exotoxin (IL-4-PE), which killed them in a concentration dependent manner. IL-4-PE also blocked colony formation of ATC cell lines in clonogenic assays. IL-4-PE mediated a significant antitumor activity in mouse models of ATC. Intratumoral administration of IL-4-PE caused significant regression of established tumors in a dose dependent manner and increased the overall survival without any visible toxicity. Thus, IL-4Rα in ATC may represent a novel therapeutic target and IL-4-PE may serve as an investigational therapeutic option for ATC.",
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AU - Leland, Pamela

AU - Varrichio, Frederick

AU - Lababidi, Samir

AU - Lloyd, Ricardo

AU - Kasperbauer, Jan

AU - Puri, Raj K.

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