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Kapoor: Prominin-1 and Its Role in Tumor Progression and Assessment of Clinical Prognosis in Systemic Malignancies
To the Editor:
The recent article by Di Bonito et al. [1] provided for highly stimulating reading. Prominin-1 may influence tumor progression and clinical prognosis in a number of other systemic tumors. A similar relationship is seen in colorectal cancers. In fact, prominin-1 exerts significant influence on tumor progression in colonic malignancies. Nearly, 36% of all malignant colonic masses are positive for prominin-1 expression [2]. Decreased "overall survival" is seen in patients with up-regulated prominin-1 levels. Accentuated prominin-1 expression is associated with accentuated tumor invasiveness. In general, "microsatellite instability-high" tumors express lower levels of prominin-1 in contrast to "microsatellite stable" colorectal tumors [3]. Not surprisingly, only 9% of colorectal tumors with a good prognosis are positive for prominin-1. In contrast, nearly 52% of colorectal malignancies that exhibit a poor clinical outcome are positive for prominin-1. Lymph node metastasis is also more prominent in tumors positive for prominin-1. Interestingly, the expression of prominin-1 by malignant colonic tissue is decreased following preoperative treatment with nonsteroidal anti-inflammatory agents [4].
Prominin-1 expression also plays a role in tumor progression in prostatic malignancies. For instance, tumor cells that are positive for prominin-1 expression tend to proliferate at a significantly more accentuated rate in comparison to prominin-1 negative cancer cells [5,6]. Not surprisingly, tumor cells in the G-2 phase are primarily composed of prominin-1 positive cells. A similar association is seen in ovarian malignancies. Nearly 31% of all ovarian cancers are positive for prominin-1 expression. A poor clinical prognosis is seen in patients with ovarian tumors with accentuated prominin-1 expression as is reflected in the shorter "disease-free survival" times noted in these patients [7].
The above examples illustrate the significant role that prominin-1 plays in tumor progression and its potential use as a significant prognostic maker.

Notes

The author declares that he has no competing interests.

References

1. Di Bonito M, Collina F, Cantile M, Camerlingo R, Cerrone M, Marra L, et al. Aberrant expression of cancer stem cells marker prominin-1 in low-grade tubulobular breast carcinoma: a correlative study between qRT-PCR, flow-cytometric and immunohistochemistry analysis. J Breast Cancer. 2012; 15:15–23.
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2. Wang K, Xu J, Zhang J, Huang J. Prognostic role of CD133 expression in colorectal cancer: a meta-analysis. BMC Cancer. 2012; 12:573.
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3. Park JJ, Kwon JH, Oh SH, Choi J, Moon CM, Ahn JB, et al. Differential expression of CD133 based on microsatellite instability status in human colorectal cancer. Mol Carcinog. Epub 2012 Oct 12. DOI: http://dx.doi.org/10.1002/mc.21971.
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4. Reggiani Bonetti L, Migaldi M, Caredda E, Boninsegna A, Ponz De Leon M, Di Gregorio C, et al. Increased expression of CD133 is a strong predictor of poor outcome in stage I colorectal cancer patients. Scand J Gastroenterol. 2012; 47:1211–1217.
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5. Lonnroth C, Andersson M, Nordgren S, Lundholm K. Downregulation of prominin 1/CD133 expression in colorectal cancer by NSAIDs following short-term preoperative treatment. Int J Oncol. 2012; 41:15–23.
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6. Reyes EE, Kunovac SK, Duggan R, Kregel S, Griend DJ. Growth kinetics of CD133-positive prostate cancer cells. Prostate. 2013; 73:724–733.
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7. Zhang J, Guo X, Chang DY, Rosen DG, Mercado-Uribe I, Liu J. CD133 expression associated with poor prognosis in ovarian cancer. Mod Pathol. 2012; 25:456–464.
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