Constitutive activation of a slowly migrating isoform of Stat3 in mycosis fungoides: tyrphostin AG490 inhibits Stat3 activation and growth of mycosis fungoides tumor cell lines

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Constitutive activation of a slowly migrating isoform of Stat3 in mycosis fungoides: tyrphostin AG490 inhibits Stat3 activation and growth of mycosis fungoides tumor cell lines. / Nielsen, M; Kaltoft, K; Nordahl, M; Röpke, C; Geisler, C; Mustelin, T; Dobson, P; Svejgaard, A; Odum, N.

In: Proceedings of the National Academy of Science of the United States of America, Vol. 94, No. 13, 1997, p. 6764-9.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Nielsen, M, Kaltoft, K, Nordahl, M, Röpke, C, Geisler, C, Mustelin, T, Dobson, P, Svejgaard, A & Odum, N 1997, 'Constitutive activation of a slowly migrating isoform of Stat3 in mycosis fungoides: tyrphostin AG490 inhibits Stat3 activation and growth of mycosis fungoides tumor cell lines', Proceedings of the National Academy of Science of the United States of America, vol. 94, no. 13, pp. 6764-9.

APA

Nielsen, M., Kaltoft, K., Nordahl, M., Röpke, C., Geisler, C., Mustelin, T., Dobson, P., Svejgaard, A., & Odum, N. (1997). Constitutive activation of a slowly migrating isoform of Stat3 in mycosis fungoides: tyrphostin AG490 inhibits Stat3 activation and growth of mycosis fungoides tumor cell lines. Proceedings of the National Academy of Science of the United States of America, 94(13), 6764-9.

Vancouver

Nielsen M, Kaltoft K, Nordahl M, Röpke C, Geisler C, Mustelin T et al. Constitutive activation of a slowly migrating isoform of Stat3 in mycosis fungoides: tyrphostin AG490 inhibits Stat3 activation and growth of mycosis fungoides tumor cell lines. Proceedings of the National Academy of Science of the United States of America. 1997;94(13):6764-9.

Author

Nielsen, M ; Kaltoft, K ; Nordahl, M ; Röpke, C ; Geisler, C ; Mustelin, T ; Dobson, P ; Svejgaard, A ; Odum, N. / Constitutive activation of a slowly migrating isoform of Stat3 in mycosis fungoides: tyrphostin AG490 inhibits Stat3 activation and growth of mycosis fungoides tumor cell lines. In: Proceedings of the National Academy of Science of the United States of America. 1997 ; Vol. 94, No. 13. pp. 6764-9.

Bibtex

@article{fd625cf0b0a411ddb538000ea68e967b,
title = "Constitutive activation of a slowly migrating isoform of Stat3 in mycosis fungoides: tyrphostin AG490 inhibits Stat3 activation and growth of mycosis fungoides tumor cell lines",
abstract = "Mycosis fungoides (MF) is a low-grade cutaneous T cell lymphoma of unknown etiology. In this report, the Jak/Stat (Janus kinase/signal transducer and activator of transcription) signaling pathway was investigated in tumor cell lines established from skin biopsy specimens from a patient with MF. Jaks link cytokine receptors to Stats, and abnormal Jak/Stat signaling has been observed in some hemopoietic cancers. In MF tumor cells, a slowly migrating isoform of Stat3, Stat3(sm), was found to be constitutively activated, i.e., (i) Stat3(sm) was constitutively phosphorylated on tyrosine residues, and tyrosine phosphorylation was not enhanced by growth factor stimulation; (ii) band shift assays and immunoprecipitations of DNA/Stat complexes showed constitutive DNA-binding properties of Stat3(sm); and (iii) Stat3(sm) was constitutively associated with Jak3. The abnormal activation of Stat3(sm) was highly specific. Thus, neither the fast migrating isoform of Stat3 (Stat3(fm)) nor other Stats (Stat1, Stat2, and Stat4 through Stat6) were constitutively activated. The Jak kinase inhibitor, tyrphostin AG490, blocked the constitutive activation of Stat3(sm) and inhibited spontaneous as well as interleukin 2-induced growth of MF tumor cells. In conclusion, we have provided evidence for an abnormal Jak/Stat signaling and growth regulation in tumor cells obtained from affected skin of an MF patient.",
author = "M Nielsen and K Kaltoft and M Nordahl and C R{\"o}pke and C Geisler and T Mustelin and P Dobson and A Svejgaard and N Odum",
note = "Keywords: Cell Division; DNA-Binding Proteins; Enzyme Activation; Enzyme Inhibitors; Humans; Interleukin-2; Mycosis Fungoides; Nitriles; STAT3 Transcription Factor; Signal Transduction; Skin Neoplasms; Trans-Activators; Tumor Cells, Cultured; Tyrphostins",
year = "1997",
language = "English",
volume = "94",
pages = "6764--9",
journal = "Proceedings of the National Academy of Sciences of the United States of America",
issn = "0027-8424",
publisher = "The National Academy of Sciences of the United States of America",
number = "13",

}

RIS

TY - JOUR

T1 - Constitutive activation of a slowly migrating isoform of Stat3 in mycosis fungoides: tyrphostin AG490 inhibits Stat3 activation and growth of mycosis fungoides tumor cell lines

AU - Nielsen, M

AU - Kaltoft, K

AU - Nordahl, M

AU - Röpke, C

AU - Geisler, C

AU - Mustelin, T

AU - Dobson, P

AU - Svejgaard, A

AU - Odum, N

N1 - Keywords: Cell Division; DNA-Binding Proteins; Enzyme Activation; Enzyme Inhibitors; Humans; Interleukin-2; Mycosis Fungoides; Nitriles; STAT3 Transcription Factor; Signal Transduction; Skin Neoplasms; Trans-Activators; Tumor Cells, Cultured; Tyrphostins

PY - 1997

Y1 - 1997

N2 - Mycosis fungoides (MF) is a low-grade cutaneous T cell lymphoma of unknown etiology. In this report, the Jak/Stat (Janus kinase/signal transducer and activator of transcription) signaling pathway was investigated in tumor cell lines established from skin biopsy specimens from a patient with MF. Jaks link cytokine receptors to Stats, and abnormal Jak/Stat signaling has been observed in some hemopoietic cancers. In MF tumor cells, a slowly migrating isoform of Stat3, Stat3(sm), was found to be constitutively activated, i.e., (i) Stat3(sm) was constitutively phosphorylated on tyrosine residues, and tyrosine phosphorylation was not enhanced by growth factor stimulation; (ii) band shift assays and immunoprecipitations of DNA/Stat complexes showed constitutive DNA-binding properties of Stat3(sm); and (iii) Stat3(sm) was constitutively associated with Jak3. The abnormal activation of Stat3(sm) was highly specific. Thus, neither the fast migrating isoform of Stat3 (Stat3(fm)) nor other Stats (Stat1, Stat2, and Stat4 through Stat6) were constitutively activated. The Jak kinase inhibitor, tyrphostin AG490, blocked the constitutive activation of Stat3(sm) and inhibited spontaneous as well as interleukin 2-induced growth of MF tumor cells. In conclusion, we have provided evidence for an abnormal Jak/Stat signaling and growth regulation in tumor cells obtained from affected skin of an MF patient.

AB - Mycosis fungoides (MF) is a low-grade cutaneous T cell lymphoma of unknown etiology. In this report, the Jak/Stat (Janus kinase/signal transducer and activator of transcription) signaling pathway was investigated in tumor cell lines established from skin biopsy specimens from a patient with MF. Jaks link cytokine receptors to Stats, and abnormal Jak/Stat signaling has been observed in some hemopoietic cancers. In MF tumor cells, a slowly migrating isoform of Stat3, Stat3(sm), was found to be constitutively activated, i.e., (i) Stat3(sm) was constitutively phosphorylated on tyrosine residues, and tyrosine phosphorylation was not enhanced by growth factor stimulation; (ii) band shift assays and immunoprecipitations of DNA/Stat complexes showed constitutive DNA-binding properties of Stat3(sm); and (iii) Stat3(sm) was constitutively associated with Jak3. The abnormal activation of Stat3(sm) was highly specific. Thus, neither the fast migrating isoform of Stat3 (Stat3(fm)) nor other Stats (Stat1, Stat2, and Stat4 through Stat6) were constitutively activated. The Jak kinase inhibitor, tyrphostin AG490, blocked the constitutive activation of Stat3(sm) and inhibited spontaneous as well as interleukin 2-induced growth of MF tumor cells. In conclusion, we have provided evidence for an abnormal Jak/Stat signaling and growth regulation in tumor cells obtained from affected skin of an MF patient.

M3 - Journal article

C2 - 9192639

VL - 94

SP - 6764

EP - 6769

JO - Proceedings of the National Academy of Sciences of the United States of America

JF - Proceedings of the National Academy of Sciences of the United States of America

SN - 0027-8424

IS - 13

ER -

ID: 8545645