A new hypoxia-responsive lncRNA in metastatic breast cancer
Editorial Commentary

A new hypoxia-responsive lncRNA in metastatic breast cancer

Juliet D. French, Stacey L. Edwards

QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia

Correspondence to: Stacey L. Edwards. QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia. Email: Stacey.Edwards@qimrberghofer.edu.au.

Provenance and Peer Review: This article was commissioned by the editorial office, Non-coding RNA Investigation. The article did not undergo external peer review.

Comment on: Niu Y, Bao L, Chen Y, et al. HIF-2-induced long non-coding RNA RAB11B-AS1 promotes hypoxia-mediated angiogenesis and breast cancer metastasis. Cancer Res 2020;80:964-75.


Received: 18 March 2020; Accepted: 30 March 2020; Published: 30 June 2020.

doi: 10.21037/ncri.2020.03.03


Metastatic breast cancer, refers to the spread of the disease from the breast to other parts of the body, most often to bone, brain, liver or lungs. Despite advances in breast cancer management, most cancer deaths result from metastases that are resistant to systemic therapies (1). Hypoxia (or reduced oxygen availability) is a hallmark of the breast tumor microenvironment and plays an important role in metastatic progression. Breast tumor cells adapt to hypoxia by increasing the activity of the hypoxia-inducible transcription factors (HIF1 and HIF2), which regulate the expression of target genes involved in cancer progression (2). Recent studies have implicated long non-coding RNAs (lncRNAs) in hypoxia/HIF-associated breast cancer metastasis, through various mechanisms. Notable examples include the nuclear lncRNA MALAT1 (metastasis-associated lung adenocarcinoma transcript 1), which is widely reported as a metastasis-promoting lncRNA, however a recent study provided strong evidence that MALAT1 suppresses breast cancer metastasis through inactivation of the TEAD transcription factor (3). HOTAIR (HOX transcript antisense RNA) is highly expressed in primary breast tumors and metastases and associated with poor prognosis. HOTAIR promotes epithelial to mesenchymal transition (EMT) by recruiting the polycomb repressive complex-2 (PRC2) to epigenetically silence target gene promoters (4). Furthermore, hypoxic induction of NEAT1 (nuclear paraspeckle assembly transcript 1) induces the formation of nuclear structures called paraspeckles and retention of F11R (also known as junctional adhesion molecule 1) mRNA in the nucleus (5). Induction of NEAT1 in hypoxia also leads to hallmarks of increased tumorigenesis including acceleration of tumor cell proliferation and inhibition of apoptosis (5).

The recent study by Niu et al. (6), provides another example of a hypoxia-responsive lncRNA involved in metastatic breast cancer. The authors initially used RNAseq to identify an hypoxia-inducible antisense lncRNA, called RAB11B-AS1 from MDA-MB-231 breast cancer cells under hypoxic conditions (7). Subsequent ChIP-seq and qPCR showed that HIF2, but not HIF1, was enriched at the RAB11B-AS1 promoter and responsible for hypoxia-induced lncRNA expression. Nui and colleagues then investigated the oncogenic role of RAB11B-AS1 in vitro and in vivo through gain- and loss-of function studies. They found ectopic expression of RAB11B-AS1 promoted cell migration and invasion in MDA-MB-231 and SUM159 breast cancer cells, whereas RAB11B-AS1 depletion caused the opposite effect. Orthotopic injection of MDA-MB-231 cells, ectopically expressing RAB11B-AS1, into the mammary fat pads of NSG mice, did not affect primary tumor growth, but showed increased expression of the endomucin capillary marker and extensive metastases to the lungs and liver as compared to the control group. Collectively, these results suggest that hypoxia-induced RAB11B-AS1 promotes metastasis of breast cancer cells to distant tissues.

To investigate the mechanisms by which RAB11B-AS1 contributes to angiogenesis, the authors analysed RNA-seq data from RAB11B-AS1-overexpressed MDA-MB-231 under hypoxia. Gene ontology analysis indicated multiple biological process likely contribute to the phenotype, although it was difficult to rank the results as no value for enrichment or fold-change was provided. RT-qPCR in RAB11B-AS1-overexpressed MDA-MB-231 was used to validate the RNAseq results, but it is unclear how many genes from the pathway analysis were assessed. The authors chose to highlight increased VEGFA and ANGPTL4 mRNA levels (both genes encode pro-angiogenic factors) in hypoxic breast cancer cells, although this result would be strengthened by confirming a concomitant increase in protein levels. Of note, RAB11B-AS1 and ANGPTL4 map to chromosome 19, whereas VEGFA locates to chromosome 6, suggesting RAB11B-AS1 operates either in trans to directly regulate these two genes or indirectly through other mechanisms. Notably, ectopic expression or silencing of RAB11B-AS1 did not affect the mRNA levels of the RAB11B sense transcript or other key angiogenic factors such as FGF, ANGPT2 and CXCR4, suggesting some level of trans-acting target-specificity.

The gene ontology results identified pol II gene regulation as the top biological function, suggesting RNA11B-AS1 may alter pol II regulation or function. RNA pulldown assays detected strong binding of pol II to the RNA11B-AS1 transcript in MDA-MB-231 cells under both normoxic and hypoxic conditions. ChIP-PCR then showed that pol II was enriched at the promoters of VEGFA and ANGPTL4, and this enrichment was significantly increased in hypoxic MDA-MB-231 cells. Importantly, RNA11B-AS1 depletion reduced pol II occupancy at the VEGFA and ANGPTL4 promoters, which correlated with decreased gene expression in hypoxic MDA-MB-231 cells. It is possible that RNA11B-AS1 regulates the recruitment of pol II to a subset of genes involved in hypoxia.

Of note, it is established that HIF binding also activates VEGFA and ANGPTL4 transcription in hypoxic breast cells (8,9). To explore any connection to RNA11B-AS1, Niu et al used RNA pull down assays to show that neither HIF1 or HIF2 bound to the RNA11B-AS1 transcript. In addition, ectopic expression of RNA11B-AS1 had no effect on HIF transcriptional activity in reporter assays in normoxic and hypoxic cells. However, it is not clear if a reporter construct can adequately recapitulate the chromatin environment. It will be therefore be important to show that overexpression and/or depletion of RNA11B-AS1 does not affect the recruitment of HIF to hypoxia-responsive promoters such as VEGFA and ANGPTL4.

In summary, Niu et al have characterised a hypoxia-responsive metastasis-associated lncRNA, which adds to the ever increasing list of lncRNAs involved in breast cancer progression. Mechanistically, RNA11B-AS1 likely contributes to metastasis through pol II activation of a subset of angiogenic factors including VEGFA and ANGPTL4, suggesting it functions as an oncogene. However, a recent study provided evidence that RNA11B-AS1 prevents osteosarcoma progression via suppression of RAB11B, suggesting in this context RNA11B-AS1 acts as a tumor suppressor (10). The authors suggest that RNA11B-AS1 may serve as a new therapeutic target for breast cancer. Therapeutic targeting of hypoxia and HIFs in cancer is a very active research area, however developing specific inhibitors has been challenging (11). Given the large number of lncRNAs reported to directly or indirectly regulate HIF expression (12), it is reasonable to assume that hypoxia-responsive lncRNA alterations may improve targeted strategies against metastatic breast cancer.


Acknowledgments

Funding: SLE is supported by a NHMRC Senior Research Fellowship (1135932). JDF is supported by a philanthropic donation from Isabel and Roderic Allpass.


Footnote

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/ncri.2020.03.03). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


References

  1. Gonzalez-Angulo AM, Morales-Vasquez F, Hortobagyi GN. Overview of resistance to systemic therapy in patients with breast cancer. Adv Exp Med Biol 2007;608:1-22. [Crossref] [PubMed]
  2. Rankin EB, Giaccia AJ. Hypoxic control of metastasis. Science 2016;352:175-80. [Crossref] [PubMed]
  3. Kim J, Piao HL, Kim BJ, et al. Long noncoding RNA MALAT1 suppresses breast cancer metastasis. Nat Genet 2018;50:1705-15. [Crossref] [PubMed]
  4. Gupta RA, Shah N, Wang KC, et al. Long non-coding RNA HOTAIR reprograms chromatin state to promote cancer metastasis. Nature 2010;464:1071-6. [Crossref] [PubMed]
  5. Choudhry H, Albukhari A, Morotti M, et al. Tumor hypoxia induces nuclear paraspeckle formation through HIF-2alpha dependent transcriptional activation of NEAT1 leading to cancer cell survival. Oncogene 2015;34:4546. [Crossref] [PubMed]
  6. Niu Y, Bao L, Chen Y, et al. HIF2-induced long noncoding RNA RAB11B-AS1 promotes hypoxia-mediated angiogenesis and breast cancer metastasis. Cancer Res 2020;80:964-75. [Crossref] [PubMed]
  7. Chen Y, Zhang B, Bao L, et al. ZMYND8 acetylation mediates HIF-dependent breast cancer progression and metastasis. J Clin Invest 2018;128:1937-55. [Crossref] [PubMed]
  8. Zhang H, Wong CC, Wei H, et al. HIF-1-dependent expression of angiopoietin-like 4 and L1CAM mediates vascular metastasis of hypoxic breast cancer cells to the lungs. Oncogene 2012;31:1757-70. [Crossref] [PubMed]
  9. De Francesco EM, Lappano R, Santolla MF, et al. HIF-1alpha/GPER signaling mediates the expression of VEGF induced by hypoxia in breast cancer associated fibroblasts (CAFs). Breast Cancer Res 2013;15:R64. [Crossref] [PubMed]
  10. Chen Z, Liu Z, Yang Y, et al. Long non-coding RNA RAB11B-AS1 prevents osteosarcoma development and progression via its natural antisense transcript RAB11B. Oncotarget 2018;9:26770-86. [Crossref] [PubMed]
  11. Wigerup C, Pahlman S, Bexell D. Therapeutic targeting of hypoxia and hypoxia-inducible factors in cancer. Pharmacol Ther 2016;164:152-69. [Crossref] [PubMed]
  12. Peng X, Gao H, Xu R, et al. The interplay between HIF-1alpha and noncoding RNAs in cancer. J Exp Clin Cancer Res 2020;39:27. [Crossref] [PubMed]
doi: 10.21037/ncri.2020.03.03
Cite this article as: French JD, Edwards SL. A new hypoxia-responsive lncRNA in metastatic breast cancer. Non-coding RNA Investig 2020;4:5.