Pituitary tumor-transforming gene (PTTG): a novel target for anti-tumor therapy.

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Pituitary tumor-transforming gene (PTTG): a novel target for anti-tumor therapy. / Solbach, Christine; Roller, Marc; Peters, Silke; Nicoletti, Maria; Kaufmann, Manfred; Knecht, Rainald.

In: ANTICANCER RES, Vol. 25, No. 1, 1, 2005, p. 121-125.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Solbach, C, Roller, M, Peters, S, Nicoletti, M, Kaufmann, M & Knecht, R 2005, 'Pituitary tumor-transforming gene (PTTG): a novel target for anti-tumor therapy.', ANTICANCER RES, vol. 25, no. 1, 1, pp. 121-125. <http://www.ncbi.nlm.nih.gov/pubmed/15816528?dopt=Citation>

APA

Solbach, C., Roller, M., Peters, S., Nicoletti, M., Kaufmann, M., & Knecht, R. (2005). Pituitary tumor-transforming gene (PTTG): a novel target for anti-tumor therapy. ANTICANCER RES, 25(1), 121-125. [1]. http://www.ncbi.nlm.nih.gov/pubmed/15816528?dopt=Citation

Vancouver

Solbach C, Roller M, Peters S, Nicoletti M, Kaufmann M, Knecht R. Pituitary tumor-transforming gene (PTTG): a novel target for anti-tumor therapy. ANTICANCER RES. 2005;25(1):121-125. 1.

Bibtex

@article{630b6688bfac4a14aa66273aba517291,
title = "Pituitary tumor-transforming gene (PTTG): a novel target for anti-tumor therapy.",
abstract = "BACKGROUND: The proto-oncogene pituitary tumor-transforming gene (PTTG) is described as abundantly over-expressed in a variety of neoplasms with impact on neovascularization and tumor invasiveness. Based on these findings, we raised the question as to whether PTTG is a target for an anti-tumor therapy. MATERIALS AND METHODS: To investigate the impact of PTTG depletion on the human cervical cancer cell line HELA-S3, we used antisense-oligodesoxynucleotides (antisense-ODNs) and subjected them to in vitro transfection experiments. The PTTG mRNA level was determined by RT-PCR (45 cycles) and PTTG protein levels were determined by Western blot experiments. The impact of PTTG depletion on cell growth was determined 24, 48 and 72 hours post transfection by the trypan blue exclusion method. RESULTS: We found an antisense-ODN effective in down-regulation of PTTG mRNA and protein level. Furthermore, transfection resulted in a significant growth inhibitory effect as well as an increased level of apoptotic figures. CONCLUSION: Our studies revealed an anti-tumor potential for this target in cancer therapy.",
author = "Christine Solbach and Marc Roller and Silke Peters and Maria Nicoletti and Manfred Kaufmann and Rainald Knecht",
year = "2005",
language = "Deutsch",
volume = "25",
pages = "121--125",
journal = "ANTICANCER RES",
issn = "0250-7005",
publisher = "International Institute of Anticancer Research",
number = "1",

}

RIS

TY - JOUR

T1 - Pituitary tumor-transforming gene (PTTG): a novel target for anti-tumor therapy.

AU - Solbach, Christine

AU - Roller, Marc

AU - Peters, Silke

AU - Nicoletti, Maria

AU - Kaufmann, Manfred

AU - Knecht, Rainald

PY - 2005

Y1 - 2005

N2 - BACKGROUND: The proto-oncogene pituitary tumor-transforming gene (PTTG) is described as abundantly over-expressed in a variety of neoplasms with impact on neovascularization and tumor invasiveness. Based on these findings, we raised the question as to whether PTTG is a target for an anti-tumor therapy. MATERIALS AND METHODS: To investigate the impact of PTTG depletion on the human cervical cancer cell line HELA-S3, we used antisense-oligodesoxynucleotides (antisense-ODNs) and subjected them to in vitro transfection experiments. The PTTG mRNA level was determined by RT-PCR (45 cycles) and PTTG protein levels were determined by Western blot experiments. The impact of PTTG depletion on cell growth was determined 24, 48 and 72 hours post transfection by the trypan blue exclusion method. RESULTS: We found an antisense-ODN effective in down-regulation of PTTG mRNA and protein level. Furthermore, transfection resulted in a significant growth inhibitory effect as well as an increased level of apoptotic figures. CONCLUSION: Our studies revealed an anti-tumor potential for this target in cancer therapy.

AB - BACKGROUND: The proto-oncogene pituitary tumor-transforming gene (PTTG) is described as abundantly over-expressed in a variety of neoplasms with impact on neovascularization and tumor invasiveness. Based on these findings, we raised the question as to whether PTTG is a target for an anti-tumor therapy. MATERIALS AND METHODS: To investigate the impact of PTTG depletion on the human cervical cancer cell line HELA-S3, we used antisense-oligodesoxynucleotides (antisense-ODNs) and subjected them to in vitro transfection experiments. The PTTG mRNA level was determined by RT-PCR (45 cycles) and PTTG protein levels were determined by Western blot experiments. The impact of PTTG depletion on cell growth was determined 24, 48 and 72 hours post transfection by the trypan blue exclusion method. RESULTS: We found an antisense-ODN effective in down-regulation of PTTG mRNA and protein level. Furthermore, transfection resulted in a significant growth inhibitory effect as well as an increased level of apoptotic figures. CONCLUSION: Our studies revealed an anti-tumor potential for this target in cancer therapy.

M3 - SCORING: Zeitschriftenaufsatz

VL - 25

SP - 121

EP - 125

JO - ANTICANCER RES

JF - ANTICANCER RES

SN - 0250-7005

IS - 1

M1 - 1

ER -