wait-and-see

宁静纯我心 感得事物人 写朴实清新. 闲书闲话养闲心,闲笔闲写记闲人;人生无虞懂珍惜,以沫相濡字字真。
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Wait-and-see? Watch-and-wait?

What can you do with cancer? It's under-treatment; it's now over-treatment - a scary journey upon talking about cancer. If you change the concept, not near-death, or dead now disease; let say, it's a chronicle, a aging disease - don't you feel better? As you have more time to deal with, you can afford "Wait-and-see? Watch-and-wait?"

The hardest to treat, not a disease, but perception - change the perception, you may have a better idea. Your brain, your heart, gotta change!


See comment in PubMed Commons below

Curr Stem Cell Res Ther. 2017 Mar 6. doi:

10.2174/1574888X12666170307105941. [Epub ahead of print]

Tissue elasticity bridges cancer stem cells to the tumor

microenvironment through microRNAs: Implications for a


"watch-and-wait" approach to cancer.

Kabeer MH1, Loudon WG1, Dethlefs BA1, Li Z2, Zhong JF2, Luo JJ3, Vu LT1, Li SC4.

Author information

1Neuro-Oncology and Stem Cell Research Laboratory, Center for

Neuroscience Research, CHOC Children`s Hospital Research Institute,


1201 West La Veta Ave., Orange, CA 92868. United States.2Division of

Periodontology, Diagnostic Sciences & Dental Hygiene and Biomedical

Sciences, Ostrow School of Dentistry, University of Southern

California, Los Angeles, CA 90089. United States.3AB Sciex, Inc.,

Brea, CA 90631. United States.4University of California Irvine School


of Medicine - CHOC Children`s Hospital- Orange, CA. United States.

Abstract

Targeting the tumor microenvironment (TME) through which cancer stem

cells (CSCs) crosstalk for cancer initiation and progression, may open

up new treatments different from those centered on the original


hallmarks of cancer genetics, which are specific for (CSCs). Cancer is

dynamic, heterogeneous, evolving with the TME and can be influenced by

tissue-specific elasticity. One of the mediators and modulators of the

crosstalk between CSCs and mechanical forces is miRNA, which can be

developmentally regulated, tissue- and cell-specific. Here, based on


our previous data, we provide a framework through which such gene

expression changes in response to external mechanical forces can be

understood during cancer progression. Recognizing the ways mechanical

forces regulate and affect intracellular signals has applications in

cancer stem cell biology. Such TME-targeted pathways shed new light on


attacking cancer stem cells with fewer side effects than traditional

gene-based treatments for cancer, requiring a "watch-and-wait"

approach. We attempt to address both normal brain microenvironment and

tumor microenvironment as both works together, intertwining in

pathology and physiology - a balance that needs to be maintaining for


the "watch-and-wait" approach to cancer.

Copyright© Bentham Science Publishers; For any queries, please email

at epub@benthamscience.org.

KEYWORDS:

Tissue elasticity; cancer stem cells; gene expression; miRNAs


PMID: 28270089 DOI: 10.2174/1574888X12666170307105941

https://www.ncbi.nlm.nih.gov/pubmed/28270089

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