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Erschienen in: Pathology & Oncology Research 3/2013

01.07.2013 | Research

Relationship Between Gastric Cancer Tau Protein Expression and Paclitaxel Sensitivity

verfasst von: Qiong Wang, Nanyao Wang, Guoyi Shao, Jianzhong Qian, Dong Shen, Yanhua Fei, Weidong Mao, Dan Wu

Erschienen in: Pathology & Oncology Research | Ausgabe 3/2013

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Abstract

The abnormal expression of Tau protein in breast cancer tissue affects paclitaxel sensitivity. The abnormal expression also exists in gastric carcinoma. Therefore, we speculate that the expression levels of Tau protein is closely related to paclitaxel sensitivity in gastric cancer, thus affecting the efficacy of paclitaxel. In this study, we used immunohistochemical methods to detect Tau protein expression levels in 47 cases of gastric cancer specimens. We also used Western blot to detect the level of Tau protein expression in gastric cancer cell lines and to check the efficacy of paclitaxel in vitro application. Findings indicate that Tau protein expression rate can reach as high as (+ +–+ + +) 63.83 % in gastric cancer. Paclitaxel induces inhibition and apoptosis with low expression of Tau protein in gastric cancer cell lines (P < 0.05). The level of Tau protein expression is significantly correlated with paclitaxel efficacy. If confirmed by further studies, the Tau protein can be another useful marker of gastric cancer, thereby leading to the application of paclitaxel in cancer treatment.
Literatur
1.
Zurück zum Zitat Zheng LZ, Chen Q (2005) Gastric cancer chemotherapy status. Gastroenterology 10:178–181 Zheng LZ, Chen Q (2005) Gastric cancer chemotherapy status. Gastroenterology 10:178–181
2.
Zurück zum Zitat Koizumi W (2005) Available options in chemotherapy for advanced gastric cancer: the current developments in Japan. Expert Opin Pharmacother 6:225–231PubMedCrossRef Koizumi W (2005) Available options in chemotherapy for advanced gastric cancer: the current developments in Japan. Expert Opin Pharmacother 6:225–231PubMedCrossRef
3.
Zurück zum Zitat Scartozzi M, Galizia E, Verdecchia L et al (2007) Chemotherapy for advanced gastric cancer: across the years for a standard of care. Expert Opin Pharmaeother 8:797–808CrossRef Scartozzi M, Galizia E, Verdecchia L et al (2007) Chemotherapy for advanced gastric cancer: across the years for a standard of care. Expert Opin Pharmaeother 8:797–808CrossRef
4.
Zurück zum Zitat Gu Y, Oyama F, Ihara Y et al (1996) Tau is widely expressed in rat tissues. J Neurochem 67:1235–1244PubMedCrossRef Gu Y, Oyama F, Ihara Y et al (1996) Tau is widely expressed in rat tissues. J Neurochem 67:1235–1244PubMedCrossRef
5.
Zurück zum Zitat Shen ZL, Qu MH, He HJ et al (2008) HeLa, HEK293, SH-SY5Y, Tau protein in cells. Res Prog Biochem Biophys 35:1364–1370 Shen ZL, Qu MH, He HJ et al (2008) HeLa, HEK293, SH-SY5Y, Tau protein in cells. Res Prog Biochem Biophys 35:1364–1370
6.
Zurück zum Zitat Muszyńska-Roslan K, Krawczuk-Rybak M, Protas PT et al (2006) Level of Tau protein in children treated for acute lymphoblastic leukemia. Pediatr Neurol 34:367–371PubMedCrossRef Muszyńska-Roslan K, Krawczuk-Rybak M, Protas PT et al (2006) Level of Tau protein in children treated for acute lymphoblastic leukemia. Pediatr Neurol 34:367–371PubMedCrossRef
7.
Zurück zum Zitat Van CE, Moiseyenko VM, Tjulandin S et al (2006) Phase Ul study of docetaxel and eisplatin plus fluorouracil compared with eisphtin and fluorouracil as first-line therapy for advanced gastric cancer: a report of the V325 study group. J Clin Oncol 24:4991–4997CrossRef Van CE, Moiseyenko VM, Tjulandin S et al (2006) Phase Ul study of docetaxel and eisplatin plus fluorouracil compared with eisphtin and fluorouracil as first-line therapy for advanced gastric cancer: a report of the V325 study group. J Clin Oncol 24:4991–4997CrossRef
8.
Zurück zum Zitat Yan S (2006) Antitumor handbook. Beijing: Peking University Medical Press 11:178 Yan S (2006) Antitumor handbook. Beijing: Peking University Medical Press 11:178
9.
Zurück zum Zitat Wang F, Han R (2002) Development of research for drug-resistance mechanism of taxol. Ai Zheng 21:439–442PubMed Wang F, Han R (2002) Development of research for drug-resistance mechanism of taxol. Ai Zheng 21:439–442PubMed
10.
Zurück zum Zitat Li Z, Wang LM, Geng MY (2006) Tau protein and nerve cell death. Chin Clinical Rehabilitation 10:124–126 Li Z, Wang LM, Geng MY (2006) Tau protein and nerve cell death. Chin Clinical Rehabilitation 10:124–126
11.
Zurück zum Zitat Rossi G, Dalpra L, Crosti F et al (2008) A new function of microtubule-associated protein tau: involvement in chromosome stability. Cell Cycle 7:1788–1794PubMedCrossRef Rossi G, Dalpra L, Crosti F et al (2008) A new function of microtubule-associated protein tau: involvement in chromosome stability. Cell Cycle 7:1788–1794PubMedCrossRef
12.
Zurück zum Zitat Pentheroudakis G, Kalogeras KT, Wirtz RM et al (2009) Gene expression of estrogen receptor, progesterone receptor and microtubule-associated protein Tau in high-risk early breast cancer: a quest for molecular predictors of treatment benefit in the context of a Hellenic Cooperative Oncology Group trial. Breast Cancer Res Treat 116:131–143PubMedCrossRef Pentheroudakis G, Kalogeras KT, Wirtz RM et al (2009) Gene expression of estrogen receptor, progesterone receptor and microtubule-associated protein Tau in high-risk early breast cancer: a quest for molecular predictors of treatment benefit in the context of a Hellenic Cooperative Oncology Group trial. Breast Cancer Res Treat 116:131–143PubMedCrossRef
13.
Zurück zum Zitat Pusztai L, Jeong JH, Gong Y et al (2009) Evaluation of microtubule-associated protein-Tau expression as a prognostic and predictive marker in the NSABP-B 28 randomized clinical trial. J Clin Oncol 10:4287–4292CrossRef Pusztai L, Jeong JH, Gong Y et al (2009) Evaluation of microtubule-associated protein-Tau expression as a prognostic and predictive marker in the NSABP-B 28 randomized clinical trial. J Clin Oncol 10:4287–4292CrossRef
14.
Zurück zum Zitat Andre F, Hatzis C, Anderson K et al (2007) Microtubule-associated protein-tau is a bifunctional predictor of endocrine sensitivity and chemotherapy resistance in estrogen receptor-positive breast cancer. Clin Cancer Res 13:2061–2067PubMedCrossRef Andre F, Hatzis C, Anderson K et al (2007) Microtubule-associated protein-tau is a bifunctional predictor of endocrine sensitivity and chemotherapy resistance in estrogen receptor-positive breast cancer. Clin Cancer Res 13:2061–2067PubMedCrossRef
15.
Zurück zum Zitat Wagner P, Wang B, Clark E et al (2005) Microtubule Associated Protein (MAP)-Tau: a novel mediator of paclitaxel sensitivity in vitro and in vivo. Cell Cycle 4:1149–1152PubMedCrossRef Wagner P, Wang B, Clark E et al (2005) Microtubule Associated Protein (MAP)-Tau: a novel mediator of paclitaxel sensitivity in vitro and in vivo. Cell Cycle 4:1149–1152PubMedCrossRef
16.
Zurück zum Zitat Rouzier R, Rajan R, Wagner P et al (2005) Microtubule-associated protein tau: a marker of paclitaxel sensitivity in breast cancer. Proc Natl Acad Sci USA 102:8315–8320PubMedCrossRef Rouzier R, Rajan R, Wagner P et al (2005) Microtubule-associated protein tau: a marker of paclitaxel sensitivity in breast cancer. Proc Natl Acad Sci USA 102:8315–8320PubMedCrossRef
17.
Zurück zum Zitat Chambonniere ML, Mosnier-Damet M, Mosnier JF et al (2001) Expression of microtubule-associated protein tau by gastrointestinal stromal tumors. Hum Pathol 32:1166–1173PubMedCrossRef Chambonniere ML, Mosnier-Damet M, Mosnier JF et al (2001) Expression of microtubule-associated protein tau by gastrointestinal stromal tumors. Hum Pathol 32:1166–1173PubMedCrossRef
18.
Zurück zum Zitat Mimori K, Sadanaga N, Yoshikawa Y et al (2006) Reduced tau expression in gastric cancer can identify candidates for successful Paclitaxel treatment. Br J Cancer 94:1894–1897PubMedCrossRef Mimori K, Sadanaga N, Yoshikawa Y et al (2006) Reduced tau expression in gastric cancer can identify candidates for successful Paclitaxel treatment. Br J Cancer 94:1894–1897PubMedCrossRef
19.
Zurück zum Zitat Feng R, Bao YZ, Peng CW et al (2010) Tau gene expression and sensitivity of gastric cancer in paclitaxel treatment. Theory Pract Surg 15:432–437 Feng R, Bao YZ, Peng CW et al (2010) Tau gene expression and sensitivity of gastric cancer in paclitaxel treatment. Theory Pract Surg 15:432–437
20.
Zurück zum Zitat Qiu LX, Qian XP, Liu B (2009) Research progress on Taxane drug efficacy forecast molecular. Modern Oncol 17:1583–1584 Qiu LX, Qian XP, Liu B (2009) Research progress on Taxane drug efficacy forecast molecular. Modern Oncol 17:1583–1584
Metadaten
Titel
Relationship Between Gastric Cancer Tau Protein Expression and Paclitaxel Sensitivity
verfasst von
Qiong Wang
Nanyao Wang
Guoyi Shao
Jianzhong Qian
Dong Shen
Yanhua Fei
Weidong Mao
Dan Wu
Publikationsdatum
01.07.2013
Verlag
Springer Netherlands
Erschienen in
Pathology & Oncology Research / Ausgabe 3/2013
Print ISSN: 1219-4956
Elektronische ISSN: 1532-2807
DOI
https://doi.org/10.1007/s12253-012-9598-5

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