Inhibitors of indoleamine 2,3-dioxygenase (IDO), a tryptophan-catabolizing enzyme that induces immune tolerance, are being assessed in clinical trials as a potential treatment for recurrent or refractory solid tumors. Clear genetic rationale for these trials, together with evidence that primary and metastatic lung tumors might be particularly susceptible to the drugs, is now reported in a preclinical study published in Cancer Discovery, a journal of the American Association for Cancer Research.
The reported data provide preclinical genetic validation for the ongoing clinical trials testing IDO inhibitors in cancer patients, according to Alexander Muller, PhD, associate professor at Lankenau Institute for Medical Research (LIMR) in Wynnewood, PA, USA. The researchers also believe that their results indicate that these drugs could have particular impact in patients with lung adenocarcinoma and lung metastases, conditions for which there is a need for new therapeutic options.
The ongoing clinical trials were initiated based on pharmacological studies that indicated that IDO inhibitors can enhance the effectiveness of other therapies in mouse models of cancer. Genetic evidence to support the concept was lacking. Muller and his colleagues, therefore, set out to determine the effect of disrupting the IDO gene on tumor development in mice.
KRAS-induced lung carcinoma
It was very important to use models of disease as physiologically relevant as possible. The researchers chose the KRAS-induced lung carcinoma model as a model of primary disease since tumors can be induced selectively in the lung and are driven by mutations in a gene known to be affected in approximately 20% of non-small cell lung cancers. They modelled metastatic disease using the 4T1 mouse breast cancer cell line, which very efficiently metastasizes to the lung after being engrafted in the mammary glands of mice. This is one of only a few breast cancer models with the capacity to metastasize efficiently to sites affected in human breast cancer patients.
Lung tumor burden
Genetically-induced IDO deficiency reduced lung tumor burden and improved survival in both models. The genetic confirmation of the importance of IDO in lung tumor development is essential support for the clinical trials. The researchers are also hoping to garner insight into the mechanisms by which IDO impacts tumor development. In this regard, their findings linking IDO to increased vascularization and modification of the inflammatory environment are critical. These data indicate that IDO has a far more expansive role in tumorigenesis than they might have thought.
IDO-sufficient and -deficient
Analysis of differences between the lungs of IDO-sufficient and -deficient tumor-bearing mice in the KRAS-induced lung carcinoma model revealed that levels of the pro-inflammatory molecule IL-6 were markedly lower in the absence of IDO. Levels of this known tumor-promoting factor were also lower in the model of metastasis when IDO was absent.
Additional work in the model of metastasis indicated that IDO-potentiated IL-6 production and promoted metastasis to the lung by driving the expansion and immunosuppressive function of a population of cells known as myeloid-derived suppressor cells. These cells are well-characterized, potent inhibitors of antitumor immune responses.
- Smith C, Chang MY, Parker KH, Beury DW, Duhadaway JB, Flick HE, et al. IDO Is a Nodal Pathogenic Driver of Lung Cancer and Metastasis Development. Cancer Discov. 2012 Jul 26. [Epub ahead of print]
- Novitskiy SV, Moses HL. Turn Off the IDO: Will Clinical Trials Be Successful? Cancer Discov. August 2012 2; 673
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