Biology:HOXA11-AS1

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Short description: Long non-coding RNA from the antisense strand in the homeobox A (HOXA gene).

HOXA11-AS lncRNA is a long non-coding RNA from the antisense strand in the homeobox A (HOXA gene). The HOX gene contains four clusters (A, B, C, and D). The sense strand of the HOXA gene codes for proteins. Alternative names for HOXA11-AS lncRNA are: HOXA-AS5, HOXA11S, HOXA11-AS1, HOXA11AS, or NCRNA00076. This gene is 3,885 nucleotides long and resides at chromosome 7 (7p15.2) and is transcribed from an independent gene promoter.[1][2] Being a lncRNA, it is longer than 200 nucleotides in length, in contrast to regular non-coding RNAs.[3]

The HOX genes code for transcription factors that are key to embryonic development.[4] This lncRNA is one of the three lncRNAs present in the 5-prime region of the HOXA11 gene. The other two lncRNAs are HOXA10-AS and HOTTIP. Of these lncRNAs, HOXA11-AS, is the most conserved sequence in a wide range of organisms, which shows its longevity in the phylogenetic tree.[5] Since HOX genes play a prominent role in embryogenesis and carcinogenesis, genes on the sense strand and antisense non-coding RNA (ncRNA) genes are often studied in their role of aberrant epithelial differentiation and cancer development.[5]

Location of HOXA11AS1 locus on chromosome 7

Function

Many lncRNAs are sequences that regulate the expression of nearby or distant genes. Common in HOX genes, lncRNAs can either regulate through cis or trans mechanisms, respectively.[6] Cis mechanisms are transcription based when nearby genes are regulated, whereas trans mechanisms are transcript-based and regulate genes afar.[4][6] HOXA11-AS regulates transcription factors and is a co-activator of the HOXA gene and other genes. Coming from HOXA homeobox, HOXA11-AS lncRNA regulates HOXA11 mRNA by blocking transcription.[7]

HOXA11-AS is similar to other lncRNAs in that it can affect many genes at once, thus allowing both local and genome-wide control.[6] It is also similar because of its function in regulating cell proliferation, cell cycle, migration, apoptosis, and promoting angiogenesis.[1] Some studies have shown that overexpression causes aberrant functions of the mechanisms listed above; however, other studies have shown downregulation is the cause.[1][5]

Mechanism

Not much is known about the exact mechanism of HOXA11-AS lncRNA.[8] Studies of Drosophila however show that many intergenic regions in the HOX genes code for lncRNAs that regulate the transcription of genes.[6] Similar to other lncRNAs, HOXA11-AS lncRNA has epigenetic control over the transcription of genes. Typically found in the nucleus of cells, HOXA11-AS lncRNA regulates the recruitment of transcription factors, and thus plays a role in chromatin remodeling.[9] As with most lncRNAS, HOXA11-AS lncRNA is attached to the site of transcription through the Polymerase II ternary complex, which allows for allele specific action. This feature is not seen in proteins or small nuclear RNAs.[6] LncRNAs are concentrated in the nucleus because these sequences, contained in the intron sequences, are removed from the final mRNA transcript in mRNA processing. Sequences that are not removed make up the mRNA and are capped, polyadenylated, and exported out of the nucleus.

Above: Cis regulation of nearby genes Below: Trans regulation of distant genes

Epigenetic proteins that are involved with lncRNAs are categorized as either: writers, readers, or erasers.[6] These proteins either add epigenetic modifications, recognize epigenetic changes, or remove epigenetic modifications, respectively. LncRNAs are able to complementarily hybridize to DNA sequences in the genome, thus targeting sequences and localizing epigenetic changes.[10] Oftentimes, lncRNAs are not free-floating in the nucleus and are attached to chromosomes.[2]

Studies regarding HOX genes have found that lncRNAs are highly expressed in relation to the homeobox genes. Known antisense HOX lncRNAs, such as HOTAIR, are scaffolds where transcription factors bind, which makes them mediators of epigenetic regulation.[10][11] Furthermore, this and other HOX lncRNAs are required for the normal development of the organism and are overexpressed in different forms of cancer.[11] The overexpression of HOX lncRNA promotes cancer because it causes epigenetic regulator proteins to relocate and the chromatin of the cell to be remodeled.[10] This remodeling can cause highly regulated functions of the cell, like proliferation, migration, and apoptosis to become unrestrained.[6] Given the sparse research on the specific mechanism of HOXA11-AS lncRNA and what is known about the role of HOX genes, it may hold that HOXA11-AS lncRNAs act in a similar manner to other HOX lncRNAs.

Cancer Research

HOXA11-AS has been reported to have roles in various different cancers, including breast cancer, lung cancer, ovarian cancer, gastric cancer, colorectal cancer, glioma, and cervical cancer.[1] Some studies have indicated that lncRNAs can be markers or targeted for treatment in various types of cancers.[4]

Breast Cancer

Tissue samples of patients with breast cancer show high expression levels of HOXA11-AS, indicating its carcinogenic nature.[7][12] Evidence of over-expression of HOXA11-AS as a causative factor of cell proliferation is seen when proliferation is blocked, once the lncRNA expression is knocked-down, or removed. Manipulating or removing the expression of this lncRNA allowed scientists to halt the progression of the cell cycle and initiate cell apoptosis at common cellular checkpoints, such as G1/G0 stage.[7][12] The expression of the lnRNA was also suppressed by using small interfering RNAs (siRNA), that would degrade HOXA11-AS lnRNA transcripts. Upon doing so, cell proliferation was blocked.[7] In addition to interfering with proliferation, degradation of HOXA11-AS lncRNA with siRNA was also seen to influence cell migration and cell tumor invasion, which is cancer metastasis.[7][12] Scientists were able to determine these effects of HOXA11-AS lncRNA on breast cancer by monitoring the changes of epithelial-mesenchymal markers in the cell. Current research is looking at the potential possibility that breast cancer can be controlled or blocked by regulating the interaction between the lnRNA and epithelium/mesenchyme.[12]

Lung Cancer

In non-small cell lung cancers (NSCLC), researchers found that HOXA11-AS plays a role as an oncogene, and that patients who had decreased HOXA11-AS lncRNA had a greater survival time. In addition, HOXA11-AS lncRNA was found to be up-regulated in the lung tissue of patients with NSCLC.[1] HOXA11-AS lncRNA was found to inhibit apoptosis, promote cancer cell proliferation, promote cell migration, and activate the cell cycle.

Ovarian Cancer

HOXA11-AS lncRNA is studied in cancer research since its over-expression has been reported in epithelial ovarian cancer (EOC). In addition, on the molecular level, single nucleotide polymorphisms (SNPs) have also been observed in the lncRNA sequences of HOXA11-AS in EOC patients. Studies have shown that the SNP variants in these lncRNA sequences do not increase risk of EOC in patients, but may be the driving force of the cancer phenotype.[5]

Regularly, HOXA11-AS lncRNA is a tumor-suppressor that inhibits EOC proliferation and migration; however, in many EOC cases, researchers observed downregulation of the lncRNA in the ovarian tissue.

Gastric Cancer

HOXA11-AS has been shown to be significantly up-regulated in gastric cancer tissue cells. The increase in expression of HOXA11-AS promotes cancer cell migration, tumor cell invasion, as well as metastasis of gastric cancer cells. HOXA11-AS has also been shown to affect cell apoptosis.[13] Research that investigates the mechanism for the upregulation of HOXA11-AS shows that it specifically promotes transcription of beta-catenin through its interaction with EZH2.[14] Additionally, current research has found that HOXA11-AS interacts with miR-1297 and blocks its ability to repress EZH2 protein translation.[13]

Colorectal Cancer

Tissue samples from patients with colorectal cancer (CRC) were observed to have decreased expression of HOXA11-AS lnRNA when compared to normal colon cells.[8] Correlations were seen between patients with larger tumor size, higher carcinoembryonic antigen (CEA), and increased metastases to decreased expression of the lncRNA.[8] These metastases were tumor-node metastases (TNM) and lymphatic metastases. Lymphatic metastases is significant, as it is a common route for cancer cells to migrate to other parts of the body.[15] Scientists were able to determine the effect HOXA11-AS lnRNA had on migration by blocking the transcript with siRNA and observing decreased cell migration and invasion.[16] There was no correlation found between the migration distance and decreased HOXA11-AS lnRNA expression.[8]

See also

  • Long noncoding RNA

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 "Clinical Significance and Effect of lncRNA HOXA11-AS in NSCLC: A Study Based on Bioinformatics, In Vitro and in Vivo Verification". Scientific Reports 7 (1): 5567. July 2017. doi:10.1038/s41598-017-05856-2. PMID 28717185. Bibcode: 2017NatSR...7.5567Z. 
  2. ↑ 2.0 2.1 "The emergence of lncRNAs in cancer biology". Cancer Discovery 1 (5): 391–407. October 2011. doi:10.1158/2159-8290.CD-11-0209. PMID 22096659. 
  3. ↑ "RNA templating the epigenome: long noncoding RNAs as molecular scaffolds". Epigenetics 6 (5): 539–543. May 2011. doi:10.4161/epi.6.5.15221. PMID 21393997. 
  4. ↑ 4.0 4.1 4.2 "Long noncoding RNAs: past, present, and future". Genetics 193 (3): 651–669. March 2013. doi:10.1534/genetics.112.146704. PMID 23463798. 
  5. ↑ 5.0 5.1 5.2 5.3 "A functional variant in HOXA11-AS, a novel long non-coding RNA, inhibits the oncogenic phenotype of epithelial ovarian cancer". Oncotarget 6 (33): 34745–34757. October 2015. doi:10.18632/oncotarget.5784. PMID 26430965. 
  6. ↑ 6.0 6.1 6.2 6.3 6.4 6.5 6.6 "Transcription of bxd noncoding RNAs promoted by trithorax represses Ubx in cis by transcriptional interference". Cell 127 (6): 1209–1221. December 2006. doi:10.1016/j.cell.2006.10.039. PMID 17174895. 
  7. ↑ 7.0 7.1 7.2 7.3 7.4 "Long non‑coding RNA HOXA11‑AS promotes cell proliferation and metastasis in human breast cancer". Molecular Medicine Reports 16 (4): 4887–4894. October 2017. doi:10.3892/mmr.2017.7163. PMID 28791375. 
  8. ↑ 8.0 8.1 8.2 8.3 "Expression and clinicopathological significance of the lncRNA HOXA11-AS in colorectal cancer". Oncology Letters 12 (5): 4155–4160. November 2016. doi:10.3892/ol.2016.5129. PMID 27895785. 
  9. ↑ "The functional role of long non-coding RNAs and epigenetics". Biological Procedures Online 16: 11. 2014-09-15. doi:10.1186/1480-9222-16-11. PMID 25276098. 
  10. ↑ 10.0 10.1 10.2 Elliott, David; Ladomery, Michael (2016). Molecular Biology of RNA (Second ed.). Oxford University Press. pp. 337–354. ISBN 978-0-19-967139-7. 
  11. ↑ 11.0 11.1 "HOTAIR: an oncogenic long non-coding RNA in different cancers". Cancer Biology & Medicine 12 (1): 1–9. March 2015. doi:10.7497/j.issn.2095-3941.2015.0006. PMID 25859406. 
  12. ↑ 12.0 12.1 12.2 12.3 "Long Non-Coding RNA (LncRNA) HOXA11-AS Promotes Breast Cancer Invasion and Metastasis by Regulating Epithelial-Mesenchymal Transition". Medical Science Monitor 23: 3393–3403. July 2017. doi:10.12659/MSM.904892. PMID 28701685. 
  13. ↑ 13.0 13.1 "LncRNA HOXA11-AS Promotes Proliferation and Invasion of Gastric Cancer by Scaffolding the Chromatin Modification Factors PRC2, LSD1, and DNMT1". Cancer Research 76 (21): 6299–6310. November 2016. doi:10.1158/0008-5472.CAN-16-0356. PMID 27651312. 
  14. ↑ "Over-expressed long noncoding RNA HOXA11-AS promotes cell cycle progression and metastasis in gastric cancer". Molecular Cancer 16 (1): 82. April 2017. doi:10.1186/s12943-017-0651-6. PMID 28441948. 
  15. ↑ "TGF-β1-induced EMT promotes targeted migration of breast cancer cells through the lymphatic system by the activation of CCR7/CCL21-mediated chemotaxis". Oncogene 35 (6): 748–760. February 2016. doi:10.1038/onc.2015.133. PMID 25961925. 
  16. ↑ "The lncRNA HOXA11-AS functions as a competing endogenous RNA to regulate PADI2 expression by sponging miR-125a-5p in liver metastasis of colorectal cancer". Oncotarget 8 (41): 70642–70652. September 2017. doi:10.18632/oncotarget.19956. PMID 29050308. 



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