Skip to main content
Log in

Comparative stemness and differentiation of luminal and basal breast cancer stem cell type under glutamine‐deprivation

  • RESEARCH ARTICLE
  • Published:
Journal of Cell Communication and Signaling Aims and scope

Abstract

Glutamine (gln) metabolism has emerged as a cancer therapeutic target in past few years, however, the effect of gln-deprivation of bCSCs remains elusive in breast cancer. In this study, effect of glutamine on stemness and differentiation potential of bCSCs isolated from MCF-7 and MDAMB-231 were studied. We have shown that bCSCs differentiate into CD24+ epithelial population under gln-deprivation and demonstrated increased expression of epithelial markers such as e-cadherin, claudin-1 and decreased expression of mesenchymal protein n-cadherin. MCF-7-bCSCs showed a decrease in EpCAMhigh population whereas MDAMB-231-bCSCs increased CD44high population in response to gln-deprivation. The expression of intracellular stem cell markers such sox-2, oct-4 and nanog showed a drastic decrease in gene expression under gln-deprived MDAMB-231-bCSCs. Finally, localization of β-catenin in MCF-7 and MDAMB-231 cells showed its accumulation in cytosol or perinuclear space reducing its efficiency to transcribe downstream genes. Conclusively, our study demonstrated that gln-deprivation induces differentiation of bCSCs into epithelial subtypes and also reduces stemness of bCSCs mediated by reduced nuclear localization of β-catenin. It also suggests that basal and luminal bCSCs respond differentially towards changes in extracellular and intracellular gln. This study could significantly affect the gln targeting regimen of breast cancer therapeutics.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

References

  • Abraham BK, Fritz P, McClellan M, Hauptvogel P, Athelogou M, Brauch H (2005) Prevalence of CD44+/CD24–/low cells in breast cancer may not be associated with clinical outcome but may favor distant metastasis. Clin Cancer Res 11:1154–1159

    Article  CAS  PubMed  Google Scholar 

  • Agboola AJ, Paish EC, Rakha EA, Powe DG, Macmillan RD, Ellis IO, Green AR (2012) EpCAM expression is an indicator of recurrence in basal-like breast cancer. Breast Cancer Res Treat 133:575–582

    Article  CAS  PubMed  Google Scholar 

  • Al-Hajj M, Wicha MS, Benito-Hernandez A, Morrison SJ, Clarke MF (2003) Prospective identification of tumorigenic breast cancer cells. Proc Natl Acad Sci USA 100:3983–3988

    Article  CAS  PubMed  Google Scholar 

  • Altman BJ, Stine ZE, Dang CV (2016) From Krebs to clinic: glutamine metabolism to cancer therapy. Nat Rev Cancer 16:619–634

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bott AJ, Maimouni S, Zong W-X (2019) The pleiotropic effects of glutamine metabolism in cancer. Cancers 11:770

    Article  CAS  PubMed Central  Google Scholar 

  • Carey BW, Finley LW, Cross JR, Allis CD, Thompson CB (2015) Intracellular α-ketoglutarate maintains the pluripotency of embryonic stem cells. Nature 518:413

    Article  CAS  PubMed  Google Scholar 

  • Chae YC, Kim JH (2018) Cancer stem cell metabolism: target for cancer therapy. BMB Rep 51:319

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Chen MS, Woodward WA, Behbod F, Peddibhotla S, Alfaro MP, Buchholz TA, Rosen JM (2007) Wnt/β-catenin mediates radiation resistance of Sca1 + progenitors in an immortalized mammary gland cell line. J Cell Sci 120:468–477

    Article  CAS  PubMed  Google Scholar 

  • Choi Y-K, Park K-G (2018) Targeting glutamine metabolism for cancer treatment. Biomol Therap 26:19

    Article  CAS  Google Scholar 

  • Cooper DL, Dougherty GJ (1995) To metastasize or not? Selection of CD44 splice sites. Nat Med 1:635–637

    Article  CAS  PubMed  Google Scholar 

  • Demas DM, Demo S, Fallah Y, Clarke R, Nephew KP, Althaouse S, Sandusky G, He W, Shajahan-Haq AN (2019) Glutamine metabolism drives growth in advanced hormone receptor positive breast cancer. Front Oncol 9:686

    Article  PubMed  PubMed Central  Google Scholar 

  • El Ansari R, McIntyre A, Craze ML, Ellis IO, Rakha EA, Green AR (2018) Altered glutamine metabolism in breast cancer; subtype dependencies and alternative adaptations. Histopathology 72:183–190

    Article  PubMed  Google Scholar 

  • Gao S, Sun Y, Liu X, Zhang D, Yang X (2017) EpCAM and COX-2 expression are positively correlated in human breast cancer. Mol Med Rep 15:3755–3760

    Article  CAS  PubMed  Google Scholar 

  • Ghebeh H, Sleiman GM, Manogaran PS, Al-Mazrou A, Barhoush E, Al-Mohanna FH, Tulbah A, Al-Faqeeh K, Adra CN (2013) Profiling of normal and malignant breast tissue show CD44 high/CD24 low phenotype as a predominant stem/progenitor marker when used in combination with Ep-CAM/CD49f markers. BMC Cancer 13:289

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Giannini A, Vivanco M, Kypta R (2000) Analysis of β-catenin aggregation and localization using GFP fusion proteins: nuclear import of α-catenin by the β-catenin/Tcf complex. Exp Cell Res 255:207–220

    Article  CAS  PubMed  Google Scholar 

  • Goodison S, Urquidi V, Tarin D (1999) CD44 cell adhesion molecules. Mol Pathol 52:189

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Green SJ, Tarone G, Underhill CB (1988) Aggregation of macrophages and fibroblasts is inhibited by a monoclonal antibody to the hyaluronate receptor. Exp Cell Res 178:224–232

    Article  CAS  PubMed  Google Scholar 

  • Jariyal H, Weinberg F, Achreja A, Nagarath D, Srivastava A (2019) Synthetic lethality: a step forward for personalized medicine in cancer. Drug Discov Today 25:305–320

    Article  PubMed  Google Scholar 

  • Jazi MS, Najafi SMA (2017) Beta-catenin forms protein aggregation at high concentrations in HEK293TCells. Iran J Med Sci 42:66

    PubMed  PubMed Central  Google Scholar 

  • Kim JH, Lee KJ, Seo Y, Kwon JH, Yoon JP, Kang JY, Lee HJ, Park SJ, Hong SP, Cheon JH (2018) Effects of metformin on colorectal cancer stem cells depend on alterations in glutamine metabolism. Sci Rep 8:409

    Article  PubMed  PubMed Central  Google Scholar 

  • Kung H-N, Marks JR, Chi J-T (2011) Glutamine synthetase is a genetic determinant of cell type-specific glutamine independence in breast epithelia. PLoS Genet 7:e1002229

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lee P, Malik D, Perkons N, Huangyang P, Khare S, Rhoades S, Gong YY, Burrows M, Finan JM, Nissim I (2020) Targeting glutamine metabolism slows soft tissue sarcoma growth. Nat Commun 11:1–15

    Google Scholar 

  • Li D, Fu Z, Chen R, Zhao X, Zhou Y, Zeng B, Yu M, Zhou Q, Lin Q, Gao W (2015) Inhibition of glutamine metabolism counteracts pancreatic cancer stem cell features and sensitizes cells to radiotherapy. Oncotarget 6:31151

    Article  PubMed  PubMed Central  Google Scholar 

  • Li B, Cao Y, Meng G, Qian L, Xu T, Yan C, Luo O, Wang S, Wei J, Ding Y (2019) Targeting glutaminase 1 attenuates stemness properties in hepatocellular carcinoma by increasing reactive oxygen species and suppressing Wnt/beta-catenin pathway. EBioMedicine 39:239–254

    Article  PubMed  Google Scholar 

  • Liao J, Liu PP, Hou G, Shao J, Yang J, Liu K, Lu W, Wen S, Hu Y, Huang P (2017) Regulation of stem-like cancer cells by glutamine through β-catenin pathway mediated by redox signaling. Mol Cancer 16:51

    Article  PubMed  PubMed Central  Google Scholar 

  • Ly S, Nguyen K, Andreeff M, Battula VL (2020) Abstract P3-02-05: targeting glutamine metabolism inhibits GD2 + breast cancer stem cell function in triple negative breast cancer. AACR, Philadelphia

    Google Scholar 

  • Lyssiotis CA, Kimmelman AC (2017) Metabolic interactions in the tumor microenvironment. Trends Cell Biol 27:863–875

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Marsboom G, Zhang G-F, Pohl-avila N, Zhang Y, Yuan Y, Kang H, Hao B, Brunengraber H, Malik AB, Rehman J (2016) Glutamine metabolism regulates the pluripotency transcription factor OCT4. Cell Rep 16:323–332

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Martowicz A, Spizzo G, Gastl G, Untergasser G (2012) Phenotype-dependent effects of EpCAM expression on growth and invasion of human breast cancer cell lines. BMC Cancer 12:501

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Oburoglu L, Tardito S, Fritz V, De Barros SC, Merida P, Craveiro M, Mamede J, Cretenet G, Mongellaz C, An X (2014) Glucose and glutamine metabolism regulate human hematopoietic stem cell lineage specification. Cell Stem Cell 15:169–184

    Article  CAS  PubMed  Google Scholar 

  • Ohashi R, Kawahara K, Fujii T, Takei H, Naito Z (2016) Higher expression of EpCAM is associated with poor clinical and pathological responses in breast cancer patients undergoing neoadjuvant chemotherapy. Pathol Int 66:210–217

    Article  CAS  PubMed  Google Scholar 

  • Pan M, Reid MA, Lowman XH, Kulkarni RP, Tran TQ, Liu X, Yang Y, Hernandez-davies JE, Rosales KK, Li H (2016) Regional glutamine deficiency in tumours promotes dedifferentiation through inhibition of histone demethylation. Nat Cell Biol 18:1090

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Peiris-Pagès M, Martinez-Outschoorn UE, Pestell RG, Sotgia F, Lisanti MP (2016) Cancer stem cell metabolism. Nat Cell Biol 18:55

    Google Scholar 

  • Ramirez-Peña E, Arnold J, Shivkumar V, Joseph R, Vidya Vijay G, Den Hollander P, Bhangre N, Allegakoen P, Prasad R, Conley Z (2019) The epithelial to mesenchymal transition promotes glutamine independence by suppressing GLS2 expression. Cancers 11:1610

    Article  PubMed Central  Google Scholar 

  • Schnell U, Cirulli V, Giepmans BN (2013) EpCAM: structure and function in health and disease. Biochim Biophys Acta Biomembr 1828:1989–2001

    Article  CAS  Google Scholar 

  • Seltzer MJ, Bennett BD, Joshi AD, Gao P, Thomas AG, Ferraris DV, Tsukamoto T, Rojas CJ, Slusher BS, Rabinowitz J (2010) Inhibition of glutaminase preferentially slows growth of glioma cells with mutant IDH1. Cancer Res 70:8981–8987

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Shapiro RA, Farrell L, Srinivasan M, Curthoys N (1991) Isolation, characterization, and in vitro expression of a cDNA that encodes the kidney isoenzyme of the mitochondrial glutaminase. J Biol Chem 266:18792–18796

    Article  CAS  PubMed  Google Scholar 

  • Sleeman KE, Kendrick H, Ashworth A, Isacke CM, Smalley MJ (2006) CD24 staining of mouse mammary gland cells defines luminal epithelial, myoepithelial/basal and non-epithelial cells. Breast Cancer Res 8:R7

    Article  PubMed  Google Scholar 

  • Song M, Kim S-H, Im CY, Hwang H-J (2018) Recent development of small molecule glutaminase inhibitors. Curr Top Med Chem 18:432–443

    Article  CAS  PubMed  Google Scholar 

  • Su Y, Chang Y, Lin W, Liang C, Lee J (2015) An aberrant nuclear localization of E-cadherin is a potent inhibitor of Wnt/β-catenin-elicited promotion of the cancer stem cell phenotype. Oncogenesis 4:e157–e157

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Tohtama S, Fujita J, Hishiki T, Matsuura T, Hattori F, Ohno R, Kanazawa H, Seki T, Nakajima K, Kishino Y (2016) Glutamine oxidation is indispensable for survival of human pluripotent stem cells. Cell Metab 23:663–674

    Article  Google Scholar 

  • Underhill C, Dorfman A (1978) The role of hyaluronic acid in intercellular adhesion of cultured mouse cells. Exp Cell Res 117:155–164

    Article  CAS  PubMed  Google Scholar 

  • Unger C, Harzmann R, Muller C, Witt C, Roberts J, Sethuraman N (2005) Phase I dose escalating study of PEG-PGA and DON: a new amino acid depleting anti cancer drug approach. J Clin Oncol 23:3130–3130

    Article  Google Scholar 

  • Valkenburg KC, Graveel CR, Zylstra-Diegel CR, Zhong Z, Williams BO (2011) Wnt/β-catenin signaling in normal and cancer stem cells. Cancers 3:2050–2079

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Woodward WA, Chen MS, Behbod F, Alfaro MP, Buchholz TA, Rosen JM (2007) WNT/β-catenin mediates radiation resistance of mouse mammary progenitor cells. Proc Natl Acad Sci USA 104:618–623

    Article  CAS  PubMed  Google Scholar 

  • Wu C, Chen L, Jin S, Li H (2018) Glutaminase inhibitors: a patent review. Expert Opin Ther Pat 28:823–835

    Article  CAS  PubMed  Google Scholar 

  • Xie J, Xiao Y, Zhu X-y, Ning Z-y, Xu H-f, Wu H-m (2016) Hypoxia regulates stemness of breast cancer MDA-MB-231 cells. Med Oncol 33:42

    Article  PubMed  PubMed Central  Google Scholar 

  • Xu X, Meng Y, Li L, Xu P, Wang J, Li Z, Bian J (2018) Overview of the development of glutaminase inhibitors: achievements and future directions. J Med Chem 62:1096–1115

    Article  PubMed  Google Scholar 

  • Ye F, Qiu Y, Li L, Yang L, Cheng F, Zhang H, Wei B, Zhang Z, Sun L, Bu H, Ye F et al (2015) The presence of EpCAM-/CD49f + cells in breast cancer is associated with a poor clinical outcome. J Breast Cancer 18:242–248

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

Mrs. Monika Seervi for their technical support for flow cytometry experiments.

Funding

National Institute of Pharmaceuticals Education and Research-Ahmedabad, Department of Pharmaceutics, Ministry of Chemicals and Fertilizers, Government of India. DST-SERB Grant (ECR/2016/002038), DBT supported Ramalingaswami Grant (BT/HRD/35/02/2006).

Author information

Authors and Affiliations

Authors

Contributions

H.J. and A.S. designed the manuscript. H.J., C.G., S.A. S.G. performed the experiments. H.J. and A.S analysed the data. H.J, drafted the manuscript and A.S. edited the manuscript. All authors have read and approved the manuscript.

Corresponding author

Correspondence to Akshay Srivastava.

Ethics declarations

Conflict of interest

The authors declare they have no such interests.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the Supplementary Information.

Supplementary Information 1 (DOCX 2162 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Jariyal, H., Gupta, C., Andhale, S. et al. Comparative stemness and differentiation of luminal and basal breast cancer stem cell type under glutamine‐deprivation. J. Cell Commun. Signal. 15, 207–222 (2021). https://doi.org/10.1007/s12079-020-00603-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12079-020-00603-1

Keywords

Navigation