果氏巴貝西蟲IgG免疫熒光試劑盒

Babesia microti IgG IFA Kit

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【公司名稱】 廣州健侖生物科技有限公司
【】    楊永漢 
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然而，加州大學圣地亞哥分校醫(yī)學院和穆爾斯癌癥中心的研究人員發(fā)現，調節(jié)抗原抗體期間的干細胞活化的信號被癌細胞劫持，用來生產快速增長，更具侵略性的腫瘤。相關文章發(fā)表于2014年8月11日的《Developmental Cell》雜志上。
Cell子刊:癌細胞劫持抗原抗體干細胞活化信號來增殖的機制
抗原抗體與抗原抗體癌之間的早已知道，但抗原抗體和抗原抗體癌風險之間的關系卻很復雜。雖然有一個孩子會降低婦女在以后生活中患抗原抗體癌的風險，但是，每次抗原抗體后都會有一個抗原抗體癌的高侵襲性形式發(fā)展的短期風險增加。目前的研究表明，懷孕期間，影響干細胞行為的重要分子可能促進了這些與抗原抗體相關的更具侵襲性抗原抗體癌的發(fā)展，研究人員計劃進一步研究這一種可能性。
作者們很快指出，他們的研究結果不應該作為一個抗原抗體的理由。這個信號通路被癌細胞劫持并不能作為一個觸發(fā)抗原抗體癌的原因。相反，它可能惡化或加速由其他因素引發(fā)的癌癥，如潛在突變或遺傳傾向。
“我們的研究并沒有指出，觸發(fā)癌癥的真正原因，而是解釋了，一旦癌癥啟動會發(fā)生什么，”病理學特聘教授和研發(fā)副主席David A. Cheresh博士說。“這里有一個比喻：得癌癥，你首先要開始激活一個致癌基因，一個攜帶突變并能夠啟動癌癥的基因。這個致癌基因相當于汽車的點火開關，而被癌細胞利用的信號通路就像汽油。有了它，汽車才能啟動，這也意味著如果致癌基因還沒有開始激活，那么癌癥就不會發(fā)展。”
在本研究中，研究人員集中于一個被稱為整合素的細胞表面受體蛋白家族，它們充當關鍵的通信渠道，zui終在這家稱為β-3整合的一個成員的作用歸零。也被稱為CD61，它已經與轉移和抗腫瘤的藥物有關。
作者指出，CD61可以作為顯示參與懷孕和癌癥期間抗原抗體發(fā)育的信號通路的良好標志。它很容易被檢測到，并可以用來診斷和治療乳房癌病例。

However, researchers at the University of California San Diego School of Medicine and the Moores Cancer Center found that signals that regulate stem cell activation during antigen-antibody abstraction were hijacked by cancer cells to produce rapidly-growing, more aggressive tumors. Related article was published in Developmental Cell magazine on August 11, 2014.
Cell Subcategory: Mechanisms of Proliferation of Cancer Cells Hijacking Antigen-derived Antibody Stem Cells
The link between antigen and antigen-antibody cancers has long been known, but the relationship between antigen-antibody and antigen-antibody cancer risk is complex. Although having one child reduces the risk of developing anti-cancer antibodies in later life, there is an increased short-term risk of development of a highly aggressive form of antigen-antibody cancer after each antigen-antibody. Current research shows that important molecules that influence stem cell behavior during pregnancy may contribute to the development of more aggressive antigen-antibody cancers associated with antigen antibodies, and the researchers plan to investigate this possibility further.
The authors quickly pointed out that their findings should not be used as a reason for antigen-antibody. This signal pathway is hijacked by cancer cells and does not serve as a trigger for antigen-antibody cancer. On the contrary, it may exacerbate or accelerate cancer caused by other factors, such as potential mutations or genetic predisposition.
"Our research did not point out the real cause of triggering cancer but explained what would happen once the cancer started," said David A. Cheresh, Ph.D., professor of pathology and vice chairman of R & D. Here's a metaphor: In cancer, you first have to start activating an oncogene, a gene that carries the mutation and activates the cancer, an oncogene that's equivalent to a car's ignition switch, and the signaling pathways used by cancer cells are like petrol. With it, the car can start, which means that if the oncogenes have not yet started to activate, then the cancer will not develop. "
In this study, researchers focused on a family of cell-surface receptor proteins called integrins that served as key communication channels and eventually zeroed in the role of a member of the family called beta-3 integration. Also known as CD61, it has been associated with metastatic and anti-tumor drugs.
The authors note that CD61 can serve as a good indicator of the signaling pathways involved in antigen and antibody development during pregnancy and cancer. It is easily detectable and can be used to diagnose and treat cases of breast cancer.