American Association for Cancer Research

April 15 Clinical Cancer Research Highlights

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Selected Articles from the April 15, 2008 Issue

The articles referenced in this Highlights section will be available online in HTML and PDF formats to all interested users at no charge until the next issue of Clinical Cancer Research is published. Click on the article title to view the complete article.

View the Table of Contents for the April 15 issue of Clinical Cancer Research.


An Immunoregulatory Enzyme Implicated in Endometrial Cancer

Ino et al.

Page 2310

Ino et al.Tumor escape from host immune surveillance is a crucial mechanism for cancer pro­gression, and an immuno­regulatory enzyme called indoleamine 2,3-dioxygenase (IDO) contributes to this tolerance mechanism in mice. To investigate the role of IDO in human cancer, Ino and colleagues studied the relationship between the level of IDO expression in tumors and the numbers of tumor-infiltrating lymphocytes or natural killer cells. They found that increased tumoral IDO expression correlated with a reduced number of tumor-infiltrating lymphocytes and natural killer cells. Further, increased tumoral IDO expression was associated with disease progression and reduced patient survival. These findings suggest that targeting IDO to restore host antitumor immunity may be a therapeutic strategy for endometrial cancer. 
 

Prognostic Value of Vascularization in Breast Cancer

Dhakal et al.

Page 2341

Vascularization is known to be important for the progression of cancer. In this study, Dhakal and colleagues investigated whether tumor vascularization has prognostic significance in patients with breast cancer. Immunostaining for the endothelial markers CD34 and CD105 and the Chalkley method were used to quantify breast cancer vascularity in 498 patients. The investigators found that combined high CD34 and CD105 counts identified patients with an unfavorable outcome. Additionally, they showed that improved identification of high-risk groups of patients can be obtained by adding CD34 and CD105 vascular analysis to other factors, such as the presence of disseminated tumor cells in marrow.  


Predicting Broad Spectrum Drug Resistance of Tumors

Efferth et al.

Page 2405

A major obstacle in treating cancer is drug resistance, which is observed in tumors from a variety of tissues, including lung, breast, and colon. To better understand drug resistance, Efferth and colleagues studied the resistance profiles of several different tumor types. They tested drugs from different classes on clinical tumor samples in vitro and found that tumors that were resistant to one drug were likely to be resistant to multiple drugs. Further, the investigators found that the resistance of a tumor to one specific drug, doxorubicin, could be used to predict whether a tumor is broadly resistant to other drugs. This work suggests that in vitro testing may be effective at predicting whether individual patients have drug-resistant tumors. 


The infiltration of T cells into a tumor is associated with a good prognosis in some types of cancer. Here, Ladoire and colleagues found that the antitumor effect of neoadjuvant chemotherapy in breast cancer is partly mediated by the immune system. Using immunohistochemistry, they studied the tumor bed immune infiltrate before and after neoadjuvant chemotherapy in 56 breast cancer patients. They found that an infiltrate enriched in cytotoxic T lymphocytes but depleted in suppressor cells after treatment is associated with complete tumor response to chemotherapy. This study highlights a role for the immune system in breast cancer patients receiving chemotherapy and suggests that T cell infiltration may be taken in account to determine the prognosis of patients. 


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