Skip to main content
Log in

Activation of STAT5-cyclin D1 Pathway in Chewing Tobacco Mediated Oral Squamous Cell Carcinoma

  • Published:
Molecular Biology Reports Aims and scope Submit manuscript

Abstract

Cyclin D1 overexpression and upregulation has been reported largely in Oral Squamous Cell Carcinoma (OSCC) but the mechanism behind it is not clear. Here, the transcription and translational upregulation of cyclin D1 was observed in most of the tobacco chewing oral cancer patients where as the gene amplification was limited to only small group (20%) of patients. A transcription factor (TF) binding site has been detected from −483 to −451 by using DNase I foot printing analysis and confirmed by electrophoretic mobility shift assay by using oral tumour nuclear extract (NE). This is a STAT binding sequence and confirmed as STAT5a by supershift assay. The binding of STAT5 was observed in 80% (24/30) oral cancer samples. The co-expression of cyclin D1 with STAT5 binding was observed in 90% (27/30) of the samples. STAT family of proteins is emerging to play role in oral carcinogenesis. Here, the binding of STAT5 might up regulate cyclin D1 in most of the samples whereas; the gene amplification events are sporadic in oral carcinogenesis. Our study provides the first evidence of the constitutive activation of STAT5-cyclin D1 pathway in chewing tobacco mediated OSCC.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. T Hunter J Pines (1991) Cell 66 IssueID6 1071–1074 Occurrence Handle10.1016/0092-8674(91)90028-W Occurrence Handle1833062

    Article  PubMed  Google Scholar 

  2. J Kato H Matsushime SW Hiebert ME Ewen CJ Sherr (1993) Genes Dev. 7 IssueID3 331–342 Occurrence Handle8449399

    PubMed  Google Scholar 

  3. G Leone J DeGregori J Jakoi JG Cook JR Nevins (1999) Proc. Natl. Acad. Sci. 96 IssueID12 6626–6631 Occurrence Handle10.1073/pnas.96.12.6626 Occurrence Handle10359762

    Article  PubMed  Google Scholar 

  4. T Motokura T Bloom HG Kim H Juppner JV Ruderman HM Kronenberg A Arnold (1991) Nature 350 IssueID6318 512–515

    Google Scholar 

  5. DA Withers RC Harvey JB Fraust O Melnyk K Carey TC Meeker (1991) Mol. Cell Biol. 11 IssueID10 4846–4853 Occurrence Handle1833629

    PubMed  Google Scholar 

  6. MI Shuster L Han MM Le Beau E Davis M Sawicki CM Lese NH Park J Colicelli SM Gollin (2000) Genes Chromosomes Cancer 28 IssueID2 153–163 Occurrence Handle10.1002/(SICI)1098-2264(200006)28:2<153::AID-GCC4>3.0.CO;2-9 Occurrence Handle10825000

    Article  PubMed  Google Scholar 

  7. K Freier S Joos C Flechtenmacher F Devens A Benner FX Bosch P Lichter C Hofele (2003) Cancer Res. 63 IssueID6 1179–1182 Occurrence Handle12649172

    PubMed  Google Scholar 

  8. X Huang SM Gollin S Raja TE Godfrey (2002) Proc. Natl. Acad. Sci. 99 IssueID17 11369–11374 Occurrence Handle10.1073/pnas.172285799 Occurrence Handle12172009

    Article  PubMed  Google Scholar 

  9. H Mineta K Miura S Takebayashi Y Ueda K Misawa H Harada M Wennerberg J Dictor (2000) Oral Oncol. 36 IssueID2 194–198 Occurrence Handle10.1016/S1368-8375(99)00078-0 Occurrence Handle10745172

    Article  PubMed  Google Scholar 

  10. M Fujii R Ishiguro T Yamashita M Tashiro (2001) Cancer Lett. 172 IssueID2 187–192 Occurrence Handle10.1016/S0304-3835(01)00651-6 Occurrence Handle11566495

    Article  PubMed  Google Scholar 

  11. R Miyamoto N Uzawa S Nagaoka K Nakakuki Y Hirata T Amagasa (2002) Cancer 95 IssueID10 2152–2159 Occurrence Handle10.1002/cncr.10929 Occurrence Handle12412169

    Article  PubMed  Google Scholar 

  12. D Nagata E Suzuki H Nishimatsu H Satonaka A Goto M Omata Y Hirata (2001) J. Biol. Chem. 276 IssueID1 662–669 Occurrence Handle10.1074/jbc.M005522200 Occurrence Handle11024050

    Article  PubMed  Google Scholar 

  13. I Matsumura T Kitamura H Wakao H Tanaka K Hashimoto C Albanese J Downward RG Pestell Y Kanakura (1999) EMBO J. 18 IssueID5 1367–1377 Occurrence Handle10.1093/emboj/18.5.1367 Occurrence Handle10064602

    Article  PubMed  Google Scholar 

  14. JI Song JR Grandis (2000) Oncogene 19 IssueID21 2489–2495 Occurrence Handle10.1038/sj.onc.1203483 Occurrence Handle10851047

    Article  PubMed  Google Scholar 

  15. JK Nagpal R Mishra BR Das (2002) Cancer 94 IssueID9 2393–2300 Occurrence Handle10.1002/cncr.10499 Occurrence Handle12015764

    Article  PubMed  Google Scholar 

  16. S Xi Q Zhang KF Dyer EC Lerner TE Smithgall WE Gooding J Kamens JR Grandis (2003) J. Biol. Chem. 278 IssueID34 31534–3183 Occurrence Handle10.1074/jbc.M303499200

    Article  Google Scholar 

  17. JE Darnell SuffixJr. (1997) Science 277 IssueID5332 1630–1635

    Google Scholar 

  18. M Masuda M Suzui R Yasumatu R Nakashima Y Kuratomi K Azuma K Tomita S Komiyama IB Weinstein (2002) Cancer Res. 62 IssueID12 3351–3355 Occurrence Handle12067972

    PubMed  Google Scholar 

  19. H Wakao F Gouilleux B Groner (1994) EMBO J. 13 IssueID9 2182–2191 Occurrence Handle7514531

    PubMed  Google Scholar 

  20. U Sen R Sankaranarayanan S Mandal AV Ramanakumar DM Parkin M Siddiqi (2002) Int. J. Cancer 100 IssueID1 86–91 Occurrence Handle10.1002/ijc.10446 Occurrence Handle12115592

    Article  PubMed  Google Scholar 

  21. Sambrook J, Fritsch EF, Maniatis T (1989). Molecular cloning – a laboratory manual 2nd ed., Cold Spring Harbour Laboratory Press.

  22. M Hattori A Tugores L Veloz M Karin DA Brenner (1990) DNA Cell Biol. 9 IssueID10 777–781 Occurrence Handle2264931

    PubMed  Google Scholar 

  23. KS Zaret JK Liu CM DiPersio (1990) Proc. Natl. Acad. Sci. 87 IssueID14 5469–5473 Occurrence Handle2371282

    PubMed  Google Scholar 

  24. MR Briggs JT Kadonaga SP Bell R Tjian (1986) Science 234 IssueID4772 47–52 Occurrence Handle3529394

    PubMed  Google Scholar 

  25. R Mishra BR Das (2003) Mol. Biol. Rep. 30 IssueID4 207–213 Occurrence Handle10.1023/A:1026384402585 Occurrence Handle14672406

    Article  PubMed  Google Scholar 

  26. RJ Bova DI Quinn JS Nankervis IE Cole BF Sheridan MJ Jensen GJ Morgan CJ Hughes RL Sutherland (1999) Clinical Cancer Res. 5 IssueID10 2810–2819

    Google Scholar 

  27. KY Lam IO Ng AP Yuen DL Kwong W Wei (2000) J. Oral. Path. Med. 29 IssueID4 167–172 Occurrence Handle10.1034/j.1600-0714.2000.290404.x

    Article  Google Scholar 

  28. H Goto K Kawano I Kobayashi H Sakai S Yanagisawa (2002) Oral Oncol. 38 IssueID6 549–556 Occurrence Handle10.1016/S1368-8375(01)00121-X Occurrence Handle12167432

    Article  PubMed  Google Scholar 

  29. A Rousseau MS Lim Z Lin RC Jordan (2001) Oral Oncol. 37 IssueID3 268–275 Occurrence Handle10.1016/S1368-8375(00)00114-7 Occurrence Handle11287281

    Article  PubMed  Google Scholar 

  30. S Magne S Caron M Charon M Rouyez I Dusanter-Fourt (2003) Mol. Cell Biol. 23 IssueID24 8934–8945 Occurrence Handle10.1128/MCB.23.24.8934-8945.2003 Occurrence Handle14645506

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Bibhu Ranjan Das.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mishra, R., Das, B.R. Activation of STAT5-cyclin D1 Pathway in Chewing Tobacco Mediated Oral Squamous Cell Carcinoma. Mol Biol Rep 32, 159–166 (2005). https://doi.org/10.1007/s11033-005-0754-9

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11033-005-0754-9

Keywords

Navigation