分析TTK/hMps1、CHK2及Ramp/L2DTL等分子在乳癌細胞中的表現情形

根據2004年統計，乳癌 (breast Cancer) 是全世界女性最常見的惡性腫瘤，也是引起女性死亡癌症的第二名。而台灣地區，乳癌是女性十大死因的第四位，所以對於乳癌的發生、治療及術後情形的進一步了解，是刻不容緩的事情。本實驗室多年來致力於乳癌的相關研究，尤其對於乳癌病患治療之後systemic recurrence的情形，更是我們探討的重點。在臨床上，乳癌病人接受乳房切除手術後，會分析乳房組織附近的淋巴結是否有癌細胞，來判斷病人術後復發的情形，根據本實驗室統計lymph node metastasis與 systemic recurrence關連性p值達0.00134，但lymph node negative的病人仍有6.4%的人會復發。由過去實驗室分析的結果顯示，p53 mutation和systemic recurrence有非常高的關連性，p值為0.00193，與臨床上以lymph node metastasis觀察systemic recurrence幾乎是相同重要，故p53 可以當作bio-marker輔助病人觀察術後復發的情形。但我們也發現有一些病人p53是正常的，但一樣會有術後復發的情形，因此才會引導我們想要更進一步探討p53 signaling pathway中相關分子，希望找其他的bio-marker來輔助觀察病人術後復發的情形。我們主要選擇了三個基因來分析，分別為TTK/hMps1、CHK2及Ramp/L2DTL，原因如下: CHK2是活化p53重要上游分子，而TTK/hMps1除了與細胞增生有關，最新研究更顯示此kinase可以活化CHK2;而Ramp/L2DTL也是與細胞增生有關的核蛋白，由Dr.許輝吉(台大病理科)之研究顯示，後者的過度表現與肝癌的轉移有關。希望藉由分析這三個基因，能找到輔助性的bio-marker幫助評估lymph node negative或p53正常但仍會術後復發的乳癌病人systemic recurrence的情形。本研究利用定序分析法檢測台灣乳癌檢體中TTK/hMps1第1638nt至2645nt的變異情形，分析結果沒有發現TTK/hMps1的特殊變異﹐卻發現兩個polymorphism（Ｉ５２７Ｉ，Ｐ７８９Ｐ）;而利用semi–quantitative RT-PCR 的方法觀察乳癌檢體中TTK/hMps1表現量，經統計結果顯示TTK/hMps1高表現量與systemic recurrence有很強的關聯性(p值達0.0022)，且與p53 mutation關聯性也很高(p值達0.0001)，故TTK/hMps1表現量高時幾乎可以當作一個bio-marker來輔助臨床上觀察病人術後復發的情形。同樣利用semi–quantitative RT-PCR 的方法觀察乳癌檢體中Ramp/L2DTL表現量，結果顯示Ramp/L2DTL高表現量與systemic recurrence也有關(p值為0.0247)，但是與病人是否會術後復發的關聯性並沒有如TTK/hMps1表現量強烈。另外利用定序分析法觀察台灣乳癌檢體中CHK2核苷酸序列的變異情形，分析結果只發現CHK2 polymorphism (E84E)，由文獻已知CHK2有11種主要不同的splice variants，經分析後發現有較特殊的splice variants，但探討 CHK2 splicing異常是否與乳癌有關，尚待進一步分析。

關鍵字

TTK/hMps1 ； CHK2 ； Ramp/L2DTL ；乳癌

並列摘要

Worldwide, breast cancer is one of the most common cancer among women, and is the second leading cause of cancer death in women as well. In Taiwan, breast cancer ranks fourth among the caures of overall female cancer-related deaths and the incidence of age in this disease tends to early onset. It is important to understand tumorgenesis and systemic recurrence in breast cancer. Our laboratory has studied the breast carcinogenesis for few years. Lymph node metastasis is a bio-marker for poor prognosis in breast cancer. However, approximately 6.4% of lymph node negative patients that acquire systemic recurrence. We are particularly interested in setting up new supplemental bio-markers for systemic recurrence. According to the previous study, p53 mutation has shown a strong correlation with recurrence (p=0.00193). p53 is a supplemental bio-marker useful for clinical diagnosis as well as lymph node metastasis. Nevertheless, there are a few wild-type p53 patients that acquired recurrence. Therefore, we examine the status of other molecular components such as CHK2 and TTK/hMps1 in the p53 signaling pathway. Inaddition, we have also analyzed the status of Ramp/L2DTL, a nuclear protein Ramp/L2DTL has shown the correlation with early metastasis of hepatoma (personal communication with Dr. H-J Hsu, NTUH). By sequence analysis, we identified two TTK/hMps1 polymorphism, Ｉ５２７Ｉand Ｐ７８９Ｐ. We determined the expression level of TTK/hMps1 by semi-quantitative RT-PCR. According to the statistical analysis, high expression level of TTK/hMps1 correlatd strongly both with systemic recurrence (p=0.0022) and p53 mutation (p=0.0001). TTK/hMps1 can be a supplemental bio-marker useful for clinical diagnosis. We also determined the expression level of Ramp/L2DTL by semi-quantitative RT-PCR. According to the resules of statistical analysis, high expression level of Ramp/L2DTL showns correlation with systemic recurrence (p=0.0247). We identified one CHK2 polymorphism (E84E) by sequencing analysis. According to the study by other groups, CHK2 with 11 major splice variants were detected in their tumor series. We have found some splice variants in breast cancer specimens. How the splice variants of CHK2 influence breast carcinogenesis remain to be addressed.

並列關鍵字

TTK/hMps1 ； CHK2 ； Ramp/L2DTL ； breast cancer

參考文獻

Bartek, J., and Lukas, J. (2003). Chk1 and Chk2 kinases in checkpoint control and cancer. Cancer Cell 3, 421-429.

Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome. Science 286, 2528-2531.

Cheung, W. M., Chu, A. H., Chu, P. W., and Ip, N. Y. (2001). Cloning and expression of a novel nuclear matrix-associated protein that is regulated during the retinoic acid-induced neuronal differentiation. J Biol Chem 276, 17083-17091.

Cornelisse, C. J., Cornelis, R. S., and Devilee, P. (1996). Genes responsible for familial breast cancer. Pathol Res Pract 192, 684-693.

Dufault, M. R., Betz, B., Wappenschmidt, B., Hofmann, W., Bandick, K., Golla, A., Pietschmann, A., Nestle-Kramling, C., Rhiem, K., Huttner, C., et al. (2004). Limited relevance of the CHEK2 gene in hereditary breast cancer. Int J Cancer 110, 320-325.

國際替代計量

分析TTK/hMps1、CHK2及Ramp/L2DTL等分子在乳癌細胞中的表現情形

全文下載

主題瀏覽