Neural stemness contributes to cell tumorigenicity

نویسندگان

چکیده

Abstract Background Previous studies demonstrated the dependence of cancer on nerve. Recently, a growing number reveal that cells share property and regulatory network with neural stem/progenitor cells. However, relationship between stemness cell tumorigenicity is unknown. Results We show cells, but not non-neural embryonic or somatic types, exhibit potential for differentiation into tissue types all germ layers when they are placed in non-native environment by transplantation immunodeficient nude mice. Likewise, capable tumor initiation have because their abilities neurosphere formation stem cell-specific serum-free medium potential, addition to neuronal was characterized previously. Moreover, loss pro-differentiation factor myoblasts, which no tumorigenicity, lead myoblast identity, gain stemness, re-differentiation. By contrast, via results tumorigenicity. These suggest contributes phenotypic heterogeneity might be an effect stemness. Bioinformatic analysis reveals genes general correlated development cancer, role development; whereas not. Most specific emerged typical species representing transition from unicellularity multicellularity during evolution. Genes Monosiga brevicollis , unicellular closest known relative metazoans, biased toward Conclusions source This due state ground hence type diversification evolution, tumorigenesis process restoration along default route pre-determined evolutionary advantage state.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Notch signaling drives stemness and tumorigenicity of esophageal adenocarcinoma.

Esophageal adenocarcinoma ranks sixth in cancer mortality in the world and its incidence has risen dramatically in the Western population over the last decades. Data presented herein strongly suggest that Notch signaling is critical for esophageal adenocarcinoma and underlies resistance to chemotherapy. We present evidence that Notch signaling drives a cancer stem cell phenotype by regulating g...

متن کامل

Tumor and Stem Cell Biology HMMR Maintains the Stemness and Tumorigenicity of Glioblastoma Stem-like Cells

Glioblastoma (GBM) stem cells (GSC) are a subpopulation of tumor cells that display stem-like characteristics (stemness) and play unique roles in tumor propagation, therapeutic resistance, and tumor recurrence. Therapeutic targets in GSCs are a focus of increasing interest to improve GBM therapy. Here we report that the hyaluronan-mediated motility receptor (HMMR) is highly expressed in GBM tum...

متن کامل

Hypoxia-regulated delta-like 1 homologue enhances cancer cell stemness and tumorigenicity.

Reduced oxygenation, or hypoxia, inhibits differentiation and facilitates stem cell maintenance. Hypoxia commonly occurs in solid tumors and promotes malignant progression. Hypoxic tumors are aggressive and exhibit stem cell-like characteristics. It remains unclear, however, whether and how hypoxia regulates cancer cell differentiation and maintains cancer cell stemness. Here, we show that hypo...

متن کامل

Tumor and Stem Cell Biology Notch Signaling Drives Stemness and Tumorigenicity of Esophageal Adenocarcinoma

Esophageal adenocarcinoma ranks sixth in cancer mortality in the world and its incidence has risen dramatically in the Western population over the last decades. Data presented herein strongly suggest that Notch signaling is critical for esophageal adenocarcinoma and underlies resistance to chemotherapy. We present evidence that Notch signaling drives a cancer stem cell phenotype by regulating g...

متن کامل

Akt-dependent activation of Erk by cyclin D1b contributes to cell invasiveness and tumorigenicity.

A total of two major isoforms, cyclin D1a and cyclin D1b, are generated from the human cyclin D1 gene by alternative splicing. Cyclin D1b is scarcely expressed in normal tissues; however, it is expressed at a high frequency in certain types of cancerous tissue. The present authors previously constructed cyclin D1b transgenic (Tg) mice and identified rectal tumors, including adenocarcinoma and s...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Cell & Bioscience

سال: 2021

ISSN: ['2045-3701']

DOI: https://doi.org/10.1186/s13578-021-00531-6