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letter
. 2013 Mar-Apr;7(3-4):85. doi: 10.5489/cuaj.741

Letter: Micro-RNA-125b and its use as a biomarker of systemic malignancies besides urothelial cancers

Shailendra Kapoor 1,
PMCID: PMC3650779  PMID: 23671519

I read with great interest the recent article by Snowdon and colleagues.1 MiR-125b may serve as a biomarker in a number of systemic malignancies besides urothelial cancers.

For instance, in non- small cell lung carcinomas (NSCLC) miR-125b expression is a significant biomarker. In fact, miR-125b expression in these malignancies is an independent determining factor of prognosis. Patients with NSCLC and high miR-125b levels typically exhibit a poor clinical outcome.2 Lower levels of miR-125b are seen in those with well differentiated tumours in comparison to those with poorly differentiated tumours. Patients with lung malignancies that do not respond to therapy typically exhibit higher levels.

Similarly, miR-125b influences clinical prognosis in colorectal malignancies. Progression of the primary tumour involves a direct involvement of miR-125b. miR-125b acts by attenuating p53 expression in the malignant cells.3 Colorectal carcinoma patients with high miR-125b levels typically have a poor clinical outcome in contrast to patients who express low levels of miR-125b. Individuals with high miR-125b expression develop larger tumours that exhibit greater invasiveness. These findings have been confirmed by Nishida and colleagues in a recent study.4

The above examples clearly illustrate the significance of assessing miR-125b levels in determining the prognosis in a number of systemic malignancies. There is a clear need for further studies to further explore the possible relationship of miR-125b with clinical prognosis in other systemic malignancies.

Footnotes

Competing interests: None declared.

References

Can Urol Assoc J. 2013 Mar-Apr;7(3-4):85–86. doi: 10.5489/cuaj.739

Response: Micro-RNA-125b and its use as a biomarker of systemic malignancies besides urothelial cancers

D Robert Siemens 1,

We appreciate the letter from Dr. Kapoor regarding the potential of miRNA gene expression, and specifically miR-125b, to allow us to create a distinct cancer signature as part of our armamentarium for diagnosis and prognosis.1 Indeed, such epigenetic fingerprinting is a hot-topic. Although our pilot results in bladder cancer, and those of others, need much more extensive external validation it is perhaps even more important that we ask the questions that need to be answered. For example, we need biomarkers that allow us to determine those high-risk, non-muscle invasive cancers that are not going to respond to intra-vesical BCG and require early cystectomy: not just the presence or absence of disease. As we continue to validate miRNA expression as a useful tool, we need to constantly focus our efforts on these clinically relevant endpoints.

Footnotes

Competing interests: None declared.

Reference


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