Related Experiment Video
Updated: Mar 2, 2026

11:02
Methods to Discover Alternative Promoter Usage and Transcriptional Regulation of Murine Bcrp1
Published on: May 27, 2016
8.6K
N-BLR, a primate-specific non-coding transcript leads to colorectal cancer invasion and migration
Isidore Rigoutsos1, Sang Kil Lee2,3, Su Youn Nam2,4
1Computational Medicine Center, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA. isidore.rigoutsos@jefferson.edu.
Genome Biology
|May 25, 2017
Summary
The primate-specific long non-coding RNA, N-BLR, promotes colorectal cancer invasion and metastasis. Its presence correlates with tumor stage and patient survival, suggesting N-BLR as a potential biomarker.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Long non-coding RNAs (ncRNAs) are increasingly recognized for their roles in cellular processes.
- N-BLR, a primate-specific ncRNA, is implicated in epithelial-to-mesenchymal transition, cell migration, and colorectal cancer invasion.
Purpose of the Study:
- To investigate the association of N-BLR abundance with colorectal cancer progression and patient survival.
- To elucidate the molecular mechanisms by which N-BLR influences cancer cell migration.
- To explore the potential of pyknon-containing loci as biomarkers.
Main Methods:
- Multivariate analyses of two independent colorectal cancer patient cohorts.
- In vitro and in vivo experiments to study N-BLR's effect on cell migration.
- Microarray analysis of pyknon-containing genomic loci expression patterns.
Main Results:
- N-BLR abundance is significantly associated with tumor stage, invasion potential, and overall survival in colorectal cancer patients.
- N-BLR facilitates migration via crosstalk with E-cadherin and ZEB1, mediated by a pyknon targeted by miR-200 family members.
- Differential expression of pyknon-containing loci observed in colorectal cancer and chronic lymphocytic leukemia tissues; several loci correlate with patient survival.
Conclusions:
- N-BLR is a novel molecular factor contributing to colorectal cancer metastasis and a potential biomarker.
- The functional pyknon in N-BLR and other pyknon-containing loci suggest a new class of primate-specific biomarkers and therapeutic targets.
Related Concept Videos
Non-LTR Retrotransposons
13.6K
As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
13.6K
lncRNA - Long Non-coding RNAs
10.0K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
10.0K
The Ras Gene
7.4K
The Ras-gene-encoded proteins are regulators of signaling pathways controlling cell proliferation, differentiation, or cell survival. The Ras-gene family in humans constitutes three primary members—the HRas, NRas, and KRas. These genes code for four functionally distinct yet closely related proteins—the HRas, NRas, KRas4A, and KRas4B. The involvement of mutant Ras genes in human cancer was first discovered in 1982 and is among the most common causes of human tumorigenesis.
Ras is a...
Ras is a...
7.4K
The Retinoblastoma Gene
4.8K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.8K
Tumor Progression
7.6K
Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
7.6K

