1. Field of the Invention
This invention relates generally to gene specific amplification, analysis and profiling of cytosolic biomolecules useful in the fields of oncology, diagnostic testing and pharmacogenomics (personalized medicine). The invention is particularly useful in such fields as cancer screening, selecting (identification and stratification of therapy responders/non-responders) and monitoring for chemotherapy treatment, or cancer recurrence.
2. Description of Related Art
The ability of tumor cells to metastasize to distant organs is responsible for most cancer deaths. In recent years, several studies have used gene expression profiling analysis on primary and metastatic tumors resulting in identification of genes having potential roles in tumor progression towards metastasis. However, despite recent advances, the molecular signaling mechanisms associated with metastasis remain poorly understood. Detection and characterization of disseminated tumor cells is beginning to aid in the dissection of the metastatic cascade, or the different events that lead to primary and secondary metastases in patients with cancer. In fact, enumeration of circulating tumor cells (CTCs) has recently been shown to be an independent predictor of progression-free survival and overall survival in patients with metastatic breast cancer (Cristofanilli, M., et al., 2004. Circulating Tumor Cells, Disease Progression, and Survival in Metastatic Breast Cancer. N. Eng. Jour Med 351, 781-791).
In addition to enumeration, many studies have been published regarding gene expression profiling of CTCs. These studies have yielded useful clinical information, but are limited to the evaluation of genes previously identified in solid tumors (O'Hara S M, et al., 2004. Multigene Reverse Transcription-PCR Profiling of Circulating Tumor Cells in Hormone-Refractory Prostate Cancer. Clin Chem. 50, 826-35.). Characterization of novel signaling mechanisms required for expression of genes prevalently expressed in CTCs will be crucial to gaining insight into the multi-step processes of tumor progression towards metastasis and should aid in the design of more targeted therapies.
A major characteristic required of metastatic cells is the ability to adapt to and survive the insults of pathophysiological stress before, during and after dissemination. Successful metastasis most likely requires the de novo expression, or activation of genes that augment survival of tumor cells during periods of pathophysiological stress such as hypoxia, loss of exogenous to growth factors, oxidative stress, immune response. Consequently, much research has been focused on characterizing genes involved in mediating the adaptive responses of tumor cells during periods of stress such as hypoxia resulting from a local decrease in blood supply. Similar studies have also associated the ability of tumor cells to survive and proliferate under hypoxic conditions with poor prognosis and resistance to radiation therapy. It is not surprising then that the molecular mechanisms associated with tumor cell survival during hypoxic conditions are now being targeted for novel therapeutic agents. Thus we feel it is important to identify and characterize clinically relevant metastatic gene markers induced in response to physiological stress.
Since breast cancer cells are particularly well known to adapt and survive periods of stress such as hypoxia (Knowles, et al., 2001. Hypoxia and Oxidative Stress in Breast Cancer: Hypoxia and tumourigenisis. Br Can Res 3, 318-322; Pugh, et al., 2001. Hypoxia and Oxidative Stress in Breast Cancer: Hypoxia Signalling Pathways. Br Can Res 3, 313-317) accompanied by serum deprivation, we developed a method to monitor the expression of a panel of genes identified as breast CTC identification markers, during exposure of breast cancer cell lines to hypoxia, serum deprivation and a combination thereof. Our invention reveals that serum deprivation alone, and especially serum deprivation in combination with hypoxia, lead to a dramatic increase in human anterior gradient-2 (Hag-2, AGR2) and intestinal trefoil factor-3 (TFF3, ITF3) mRNA expression. This invention provides a method and means into how CTC markers are regulated in vivo and could ultimately aid in the design of novel therapies targeted at blocking breast cancer metastasis.
The present invention provides a method and means for diagnosing cancer by utilizing the role of AGR2 and TFF3 metabolism to physiological stress. Tumors from breast cancer patients express higher levels of these genes when compared to normal tissue when subjected to stress. After normalization to ubiquitin, AGR2 and TFF3 expression increases (approximately 60%) of patient matched tumor samples when compared to normal tissue. This increase provides the foundation for assessing disease state, response to therapy and other prognostic values. The method is applicable in cancers with overexpression of one or both genes such as ovarian, lung and thyroid tumors, colon, stomach, rectum and prostate in an immunomagnetically enriched sample. Accordingly, breast cancer cells co-adapt the use of AGR2 and TFF3 to mediate cell survival and repair, similar to their role in normal intestinal epithelial cells.
The ability of tumor cells to metastasize to distant organs is responsible for most cancer deaths. Despite a growing amount of research, the molecular mechanisms associated with tumor progression towards metastasis remain poorly understood. In recent years, much of the research on this subject has been initiated on genes identified by techniques such as microarray analyses and proteomic profiling of tumor tissues and cell lines. These types of studies are, and will continue to be, crucial to gaining insight into the multi-step processes of tumor progression. Anterior gradient 2 (AGR2) is a recently to discovered human homologue of the secreted Xenopus laevis protein XAG-2. XAG-2 is expressed in the cement gland of Xenopus laevis and is associated with anteroposterior fate determination during early development. Sequence analysis of AGR2 revealed a predicted N-terminal cleavable secretory signal that suggests it is a secreted protein in humans as well. An increased interest in AGR2 was derived from the original finding that it is co-expressed with the estrogen receptor in breast cancer cell lines. AGR2 expression in an enriched sample of circulating tumor cells derived from breast, prostate and colon cancer patients would provide a diagnostic/prognostic tool in assessing these disease states. Thus making AGR2 a clinically relevant marker in cancer progression.
Breast cancer lines are subjected to serum starvation, hypoxia and a combination thereof. These treatments mimic conditions experienced by breast tumors during periods of pathophysiological stress resulting from decreased blood supply. Expression levels of genes, previously identified to be potential candidates for breast cancer CTC detection are measured by quantitative RT-PCR before and after stress induction for comparison. Serum deprivation alone, and especially serum deprivation in combination with hypoxia, leads to a dramatic increase in the expression of anterior gradient-2 (AGR2) and trefoil factor 3 (TFF3, ITF3) in breast cancer cells. The most dramatic induction of AGR2 and TFF3 expression is observed in the MDA-MB-231 cell line (
Chemical inhibitors of ERK1/2, JNK, p38 and PI3K were used in an attempt to better understand the signaling pathways responsible for induction is of AGR2 and TFF3 during serum deprivation and hypoxic treatment of MDA-MB-231 cells. Cells were treated with serum deprivation, hypoxia and a combination thereof for 48 hours in the presence and absence of each inhibitor. After treatment and quantitative PCR analysis, we observed that the ERK1/2 inhibitor, PD98059, was sufficient to block induction of AGR2 by serum deprivation alone and its combination with hypoxia (
Because AGR2 and TFF3 play a significant role in the response of breast cancer cells to physiological stress, it to be advantageous for breast tumors to express higher levels of these genes when compared to normal tissue. Using a commercially available cancer-profiling array to compare the expression of AGR2 and TFF3 in patient matched normal and breast cancer samples, AGR2 and TFF3 expression increases in approximately 60% of patient matched tumor samples when compared to normal tissue and after normalization to ubiquitin (
The present invention combines immunomagnetic enrichment of patient samples as discussed in U.S. Pat. No. 6,365,362 and U.S. Pat. No. 6,645,731 (both incorporated by reference) with a stress-induced induction of AGR2 and TFF3 to provide a method in cancer diagnosis.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US05/39602 | 11/3/2005 | WO | 00 | 10/16/2009 |