RETRACTED ARTICLE: PI3K/Akt pathway and Nanog maintain cancer stem cells in sarcomas

Abstract

The self-renewal transcription factor Nanog and the phosphoinositide 3-kinase (PI3K)–Akt pathway are known to be essential for maintenance of mesenchymal stem cells. We evaluated their contribution to the maintenance of CD133(+) cancer stem-like cells (CSCs) and spheroid-forming cells in patient-derived cell lines from three human sarcoma subtypes: HT1080 fibrosarcoma, SK-LMS-1 leiomyosarcoma, and DDLS8817 dedifferentiated liposarcoma. Levels of Nanog and activated Akt were significantly higher in sarcoma cells grown as spheroids or sorted for CD133 expression to enrich for CSCs. shRNA knockdown of Nanog decreased spheroid formation 10- to 14-fold, and reversed resistance to both doxorubicin and radiation in vitro and in H1080 flank xenografts. In the HT1080 xenograft model, doxorubicin and Nanog knockdown reduced tumor growth by 34% and 45%, respectively, and the combination reduced tumor growth by 74%. Using a human phospho-kinase antibody array, Akt1/2 signaling, known to regulate Nanog, was found to be highly activated in sarcoma spheroid cells compared with monolayer cells. Pharmacologic inhibition of Akt using LY294002 and Akt1/2 knockdown using shRNA in sarcoma CSCs decreased Nanog expression and spheroid formation and reversed chemotherapy resistance. Akt1/2 inhibition combined with doxorubicin treatment of HT1080 flank xenografts reduced tumor growth by 73%. Finally, in a human sarcoma tumor microarray, expression of CD133, Nanog, and phospho-Akt were 1.8- to 6.8-fold higher in tumor tissue compared with normal tissue. Together, these results indicate that the Akt1/2–Nanog pathway is critical for maintenance of sarcoma CSCs and spheroid-forming cells, supporting further exploration of this pathway as a therapeutic target in sarcoma.

Introduction

Mesenchymal tissues are derived from the mesoderm (i.e. middle layer of the embryo) and include the musculoskeletal system, circulatory and lymphatic systems, and connective tissues. Sarcomas are malignant tumors of mesenchymal tissues, with an annual incidence of approximately 15,000 new diagnoses in the United States, of which about 40% lead to fatality¹. Treatment of primary tumors often includes aggressive surgical resection and radiation therapy, but local recurrence remains a significant problem, especially for tumors in difficult locations such as the head and neck, paraspinal region, retroperitoneum, and pelvis. Up to half of patients with large, high-grade sarcomas develop distant metastases, most frequently to the lung². The efficacy of chemotherapy and radiation in treating local and distant recurrence is modest at best, and for the minority of patients who do respond, nearly all eventually develop resistance³.

Cancer stem-like cells (CSCs) in sarcomas and other cancers may be a source of therapy resistance as well as distant metastasis^4,5. CSCs share characteristics with normal adult stem cells, specifically the capacity for self-renewal and pluripotent differentiation⁶. Methods to identify CSCs include tumor initiation in immunodeficient mice, spheroid colony formation in vitro, and expression of certain cell surface markers. The most commonly identified cell surface marker for CSCs in sarcomas is CD133 (refs. ^7,8). Given there are over 80 distinct histologic subtypes of sarcoma, many have also suggested that sarcomas originate from multipotent cells such as mesenchymal stem cells⁹.

Thus, targeting CSCs is a worthy goal in the development of more effective treatments for advanced sarcomas, as such strategies would circumvent treatment resistance and prevent metastasis. CSCs may be regulated by stemness-related proteins, including Nanog, Sox2, Oct4, and c-Myc^10–13. Nanog plays a multifaceted role in pluripotency and embryonic stem cells by regulating the expression of Sox2, Oct4, KLF4, and itself¹⁴. Several reports have also found that Nanog expression drives CSC function and oncogenesis in multiple human cancers, including prostate cancer¹⁵, hepatocellular carcinoma¹⁶, leukemia, glioblastoma multiforme¹⁷, colorectal cancers¹⁸, lung cancer¹⁹, and breast cancer²⁰. Similarly, we have shown that Nanog expression correlates with response to therapy in sarcoma stem cells²¹.

Nanog is regulated by several pathways, including indirect association with the mitogen-activated protein kinase pathway²². The PI3K–Akt pathway has similarly been shown to play a key role in cancer stem cell biology²³, and some studies suggest that it may regulate the stemness and reprogramming in various solid tumors^24,25. In keeping with that conclusion, we previously showed that inhibition of PI3K significantly reduced expression of the CSC marker CD44 and the mesenchymal transdifferentiation controller Slug in gastric CSCs²⁶.

Here, we sought to examine the role of Nanog in the maintenance of stem-like properties in sarcoma CSCs and to determine if Nanog inhibition could reverse resistance to chemotherapy and radiation. Using a protein kinase array, we found that the PI3K/Akt pathway was upregulated in sarcoma CSCs. As we also found that PI3K/Akt regulates Nanog, we further investigated the role of the PI3K–Akt pathway in sarcoma CSCs.

Results

Nanog promotes stemness in human sarcoma cells

To explore the function of Nanog in sarcoma CSCs, we first examined its expression in sarcoma cells grown as spheroids, which enriches for CSCs^27–29. In all three sarcoma cell lines (HT1080 fibrosarcoma cells, SK-LMS-1 leiomyosarcoma cells, and DDLS8817 dedifferentiated liposarcoma cells), growth as spheroids increased expression of Nanog compared with that in monolayer-grown cells, while expression of other self-renewal proteins Sox2, Oct4, and c-Myc was not uniformly increased (Fig. 1A). We then assessed Nanog expression in flow-sorted CSCs, distinguished by the marker CD133 (ref. ³⁰), and Nanog expression was dramatically higher in CD133(+) cells (Fig. 1B).

Fig. 1. Nanog promotes stemness in human sarcoma cells.

A, B Western blot for self-renewal proteins Sox2, Oct4, Nanog, and c-Myc in human sarcoma cell lines grown as A monolayers and as spheroids and B after separation of spheroid cells into CD133+ and CD133− fractions. β-Actin, loading control. C, D Spheroid formation following lentiviral transduction with C Nanog or vector and D Nanog shRNA (sh.NANOG) or scramble control shRNA (sh.Scr). Scale bar, 100, 200 µm. *p < 0.05 compared to control. E Frequency and types of CD133 and Nanog alterations in sarcoma samples according to previous genomic studies from TCGA³¹, Liu and colleagues³², and University of Tokyo³³. F Kaplan–Meier curves of progression-free survival of sarcoma patients following potentially curative resection, stratified by the presence or absence of CD133 and Nanog mutation/amplification. Graphs in E, F generated using cBioPortal (http://www.https://cbioportal.mskcc.org).

To investigate whether Nanog influences spheroid formation, we stably overexpressed it by lentiviral transduction; this did not alter cell proliferation in vitro (Suppl. Fig. S1A). Nanog overexpression increased expression of CD133 (Suppl. Fig. S1B), increased spheroid formation by 23–49% (Fig. 1C), and increased spheroid size by 28–43% compared with control cells (Suppl. Fig. S1C). Conversely, stable knockdown of Nanog using shRNA, which did not alter cell proliferation (Suppl. Fig. S1D), in sarcoma spheroid cells resulted in decreased expression of CD133 as determined by western blot and immunofluorescence (Suppl. Fig. S1E, S1F). Nanog shRNA also decreased spheroid size by 71–74% (Suppl. Fig. S1G) and spheroid number by 70–81% (Fig. 1D) as compared with control cells. Together, these data show that Nanog is upregulated in sarcoma CSCs and promotes spheroid formation.

We finally confirmed the association of CD133 and Nanog gene mutations and copy number alterations in sarcomas with patient survival data in four publicly available databases (http://cancergenome.nih.gov)^31–33. The frequency of CD133 mutation or amplification in these cohorts was 0.8–1.9% and the frequency of Nanog mutation or amplification was 0.5–2.4% (Fig. 1E). Patients whose sarcomas had gene mutation or gene amplification of both CD133 and Nanog had significantly worse disease-free survival compared to patients whose sarcomas did not have gene mutation or gene amplification of CD133 and Nanog (Fig. 1F).

Nanog inhibition reverses chemotherapy and radiation resistance

As numerous studies have demonstrated that CSCs are generally resistant to chemotherapy^13,29,34 and radiation^35,36, we tested sarcoma cells’ sensitivity to these modalities in vitro and in vivo. Figure 2A shows proliferation assays for HT1080, SK-LMS-1, and DDLS8817 monolayer cells and spheroids cells treated with DMSO control or doxorubicin (1.5 μg/mL). For the three cell lines grown as monolayer cells, doxorubicin decreased proliferation by 28–38%. For the three cell lines grown as spheroids, doxorubicin decreased proliferation by only 11–15%. Figure 2B shows proliferation assays for monolayer cells and spheroids cells treated with DMSO control or 6 Gy of radiation. For the three cell lines grown as monolayer cells, radiation decreased proliferation by 38–50%. For the three cell lines grown as spheroids, radiation decreased proliferation by only 11–20%. HT1080 spheroids cells were next used to generate flank xenografts in mice. Upon reaching about 100 mm³, mice were treated every 6 days with doxorubicin 4 mg/kg or radiation 6 Gy for three total treatments. HT1080 xenografts were similarly resistant to doxorubicin and radiation. Control tumors grew to over 1000 mm³ in about 10 days while tumors treated with doxorubicin or radiation grew to over 1000 mm³ in about 18 days. These treatments also increased the percentage of CD133(+) cells in tumors (Fig. 2D), as well as expression of CD133 and Nanog (Fig. 2E, F); levels of other self-renewal proteins Sox2, Oct4, and c-Myc were unchanged as measured by western blot and immunofluorescence. To determine whether Nanog influences sarcoma chemotherapy and radiation resistance, Nanog was knocked down in all three sarcoma cells lines using shRNA; stable knockdown was confirmed by western blot (Suppl. Fig. S2). In Nanog-deficient cells (all three lines), doxorubicin and radiation reduced proliferation in spheroid cells by 86–91% and 66–75%, respectively (Fig. 3A, B). To investigate how elimination of Nanog affects susceptibility to these agents, we next measured DNA damage using ɣ-H2AX expression and apoptosis using Bcl-2 expression. In Nanog-deficient HT1080 spheroid cells, doxorubicin and radiation led to a significant increase in DNA damage and a significant reduction in apoptosis (Fig. 3C, D). The DNA damage response was confirmed by immunofluorescence for γ‐H2AX as an increased number of foci and by comet assay as an increased tail moment (Fig. 3E). Thus, these data suggest that sarcoma spheroid-forming cells are relatively resistant to chemotherapy and radiotherapy, and this resistance can be overcome by Nanog inhibition.

Fig. 2. CSCs contribute to sarcomas’ resistance to chemo- and radiotherapy.

A, B Proliferation of monolayers and spheroids following treatment with doxorubicin (Dox) or radiation therapy. C Growth curve of HT1080 fibrosarcoma xenografts in athymic nude mice treated with Dox or 6 Gy radiation. D Fluorescence-activated cell sorting (FACS) analysis for CD133+ cells in untreated control and Dox- or 6-Gy-treated tumors. E Western blot of tumor lysates for CD133, Sox2, Oct4, Nanog, and c-Myc. β-Actin is the loading control. F Immunofluorescence of tumors for CD133 (green) and Nanog (red) with DAPI (blue) staining in athymic nude mice treated with doxorubicin or 6 Gy radiation. Scale bar, 50 µm. *p < 0.05, **p < 0.01 compared to control.

Fig. 3. Nanog inhibition reverses chemo- and radiotherapy resistance.

A–D Proliferation of sarcoma cells grown as spheroids (A, C) and western blot for Nanog, Bcl-2, cleaved caspase-3, and γ-H2AX (B, D) following treatment with sh.NANOG or sh.Scr and doxorubicin (Dox) or 6 Gy radiotherapy. β-Actin, loading control. *p < 0.01 compared to control. E Immunofluorescence of sarcoma spheroid cells (HT1080, SK-LM-1). Top panel shows γ-H2AX in green. Middle panel shows γ-H2AX in green and nuclei in blue (DAPI). Bottom panel shows Comet assay in green. All photos are of different cells under specified conditions. Graphs show quantification of γ-H2AX positive staining and mean tail moment. Nuclei were stained with DAPI (4′,6-diamidino-2-phenylindole; blue).

We next evaluated the combination of Nanog knockdown and doxorubicin chemotherapy in vivo using flank xenografts of HT1080 cells that were stably transduced with Nanog shRNA or control shRNA (Fig. 4A). After tumors reached 100–150 mm³ in size, mice were randomized to treatment with either doxorubicin or PBS. Nanog shRNA and doxorubicin reduced tumor growth by 45% and 35%, respectively, while the combination of Nanog shRNA and doxorubicin inhibited tumor growth by 84% (Fig. 4B, C). The combination of Nanog shRNA and doxorubicin reduced proliferation as measured by Ki76 immunofluorescence in tumors after 14 days of treatment by only 28.4% compared to control tumors (Fig. 4D). In contrast, this combination reduced expression of CD133 and Nanog by >90% compared with controls and increased apoptosis by 17.5-fold as measured by cleaved caspase-3 expression, corresponding to 90% reduced expression of the anti-apoptotic protein Bcl-2(+) cells. Thus, Nanog inhibition overcomes chemotherapy resistance in HT1080 xenografts.

Fig. 4. Nanog knockdown restores sensitivity to chemotherapy in mouse xenograft models.

A Western blot of HT1080 cells transduced with sh.NANOG lentivirus for Nanog and β-actin. B Growth of HT1080 fibrosarcoma xenografts in athymic nude mice treated with sh.NANOG or sh.Scr and PBS or doxorubicin (Dox). C Photos of representative tumors. D Immunohistochemical analysis of tumors for Ki67 (green), CD133 (green), Nanog (white), cleaved caspase-3 (red), and Bcl-2 (yellow). Scale bar, 50 µm. *p < 0.01 compared to control.

PI3K/Akt signaling regulates Nanog expression

We next searched for signaling pathways that regulate Nanog in sarcoma CSCs and spheroid-forming cells by using a human phospho-kinase array to identify kinases and kinase substrates that were differentially phosphorylated between sarcoma cell lines grown as monolayers vs. spheroids. Following quantification by densitometric analysis, we found that phosphorylation of Akt1/2 and platelet-derived growth factor receptor β (PDGFR-β) were significantly increased in spheroids (Fig. 5A and Suppl. Fig. S3A). We confirmed that the PI3K/Akt pathway is highly activated in sarcoma spheroid-forming cells by western blot for phosphorylated Akt (T308 or S473) and total Akt1/2; phosphorylation was higher in sarcoma cells grown as spheroids compared with monolayers (Suppl. Fig. S3B) and in CD133+ compared with CD133− cells (Suppl. Fig. S3C). Akt shRNA knockdown or pharmacologic inhibition using LY294002 dramatically reduced levels of CD133 and Nanog but had no effect on levels of other stemness factors such as Sox2, Oct4, and c-Myc (Fig. 5B and Suppl. Fig. S3D). Furthermore, following separation of spheroids into CD133+ and CD133− cells, PI3K inhibition with LY294002 reduced the expression of CD133 and Nanog in CD133+ cells from all sarcoma lines (Suppl. Fig. S3E). Inhibition of the PI3K/Akt signaling pathway with LY294002 or Akt1/2 shRNA in CD133+ cells reduced spheroid formation under standard conditions (Fig. 5C) and from single cells (Fig. 5D and Suppl. Fig. S3F) by 71–77%.

Fig. 5. PI3K/Akt signaling regulates Nanog expression.

A Activated proteins in HT1080 monolayers and spheroids identified by human phospho-kinase array kit. B Western blot for indicated proteins following transduction with sh.Akt1/2 or sh.Scr in sarcoma spheroid cells. C CD133 (green) and Nanog (red) immunofluorescence with and DAPI (blue) counterstaining following treatment with PI3K inhibitor LY294002 or sh.Akt1/2 in spheroid cells. D Diameter of spheroids grown from single CD133+ cell cells showing following treatment with LY294002 or sh.Akt1/2 vs, DMSO or sh.Scr, respectively. E Proliferation of spheroid cells following treatment with sh.Akt1/2 and doxorubicin or 6 Gy radiation. β-Actin, loading control. Scale bar, 50 µm. *p < 0.01 compared to control.

We next examined whether PI3K inhibition increased the sensitivity of sarcoma cell lines grown as spheroids to doxorubicin chemotherapy and radiation. The PI3K inhibitor LY294002 inhibited growth by 31–35%, doxorubicin by 11–16%, and the combination by 77–84% (Suppl. Fig. S4A). LY294002 combined with doxorubicin led to significant induction of apoptosis, as measured by western blotting for cleaved caspase-3 and Bcl-2, in HT1080 spheroid cells (Suppl. Fig. S4B). Similar results were obtained when Akt1/2 shRNA was used in place of the PI3K inhibitor (Fig. 5E and Suppl. Fig. S4C). Akt1/2 shRNA with radiation enhanced the reduction in proliferation of HT1080, SK-LMS-1, and DDLS8817 sarcoma spheroid cells caused by 6-Gy radiation from 13–21% to 65–78% (Fig. 5E). Similar to results with doxorubicin, sh.Akt1/2 combined with radiation led to significant induction of apoptosis in HT1080 spheroid cells (Suppl. Fig. S4D). These studies demonstrate that the PI3K/Akt pathway regulates the expression of Nanog in sarcoma spheroid-forming cells and promotes CSC phenotypes such as spheroid formation and therapy resistance.

Combined Akt1/2 inhibition and chemotherapy inhibits stemness and tumor growth in vivo

To evaluate the efficacy of combining Akt1/2 inhibition with doxorubicin, we xenografted HT1080 cells stably transduced with Akt1/2 shRNA or control shRNA into the flanks of immunodeficient mice following confirmation of stable knockdown (Fig. 6A). Once tumors reached 100–150 mm³, mice were randomized and treated with doxorubicin or PBS. Akt1/2 shRNA or doxorubicin slowed tumor growth by approximately 40–50% (Fig. 6B), while the combination of Akt1/2 shRNA and doxorubicin inhibited growth by 74% without affecting body weight (Suppl. Fig. S5). After 14 days, xenografts were harvested and analyzed (Fig. 6C). The combination of Akt1/2 shRNA and doxorubicin resulted in a 13-fold increase in the apoptosis marker cleaved caspase-3 compared with control, and ≥90% decreases in expression of the CSC markers CD133 and Nanog and in the anti-apoptosis marker Bcl-2 as measured by immunofluorescence (Fig. 6D). To examine the role of Akt1/2 activation in human sarcoma CSCs and spheroid-forming cells, we assessed expression of CD133, Nanog, and phosphorylated Akt1/2 (S473) by immunostaining a commercially available tissue microarray containing 79 human sarcomas and 4 human normal tissues. Levels of CD133, Nanog, and phospho-Akt were 1.8–6.8-fold higher in tumor tissue compared with normal tissue (Fig. 6E). Thus, targeting the Akt1/2–Nanog signaling axis may be relevant to multiple types of sarcoma.

Fig. 6. Combined Akt1/2 inhibition and chemotherapy inhibits stemness and tumor growth in vivo.

A Western blot confirmation of Akt1/2 knockdown by shRNA in HT1080 cells. B Growth of HT1080 fibrosarcoma xenografts stably transduced with sh.Scr or sh.Akt1/2 in athymic nude mice treated and PBS or doxorubicin. C Photos of representative tumors. D Immunohistochemical analysis of tumors for proliferation using Ki67 (green), stemness using CD133 (green) and Nanog (white), and apoptosis using cleaved caspase-3 (red) and Bcl-2 (yellow). E Immunohistochemical staining of commercially available tissue array slide containing 79 human sarcomas and 4 human normal tissues for CD133, Nanog, and p-Akt1/2 (S473). β-Actin, loading control. Scale bar, 50 µm. *p < 0.01 compared to control.

Discussion

In this study, we demonstrate the central role of Nanog and PI3K/Akt signaling in maintaining sarcoma CSC phenotypes including spheroid formation and therapy resistance in sarcomas. Knockdown of Nanog in spheroid cells or CD133(+) cells using shRNA inhibited spheroid formation and reversed their resistance to chemotherapy and radiation. In the HT1080 flank xenograft model, inhibition of Nanog synergized with doxorubicin to reduce tumor growth, and histologic examination of treated tumors found dramatic increases in tumor cell apoptosis and depletion of CD133+ cells. Moreover, pharmacologic inhibition or knockdown of Akt in sarcoma CSCs reduced expression of Nanog, reduced spheroid formation, and reversed therapy resistance.

The existence of CSCs has been shown in multiple human cancers including several sarcoma subtypes, their potential as therapeutic targets remains less examined. Whether this population of cells is responsible for therapeutic resistance and recurrence has not been established. Sarcomas are a heterogeneous group of tumors with over 80 subtypes, each with its own tumor biology and response to therapy. However, sarcomas may originate from multipotent stem cells such as mesenchymal stem cells⁹, and so targeting such cells may have broad application to all sarcoma subtypes. Here we examined three common sarcoma subtypes (fibrosarcoma, leiomyosarcoma, and liposarcoma) and found similar effects when targeting Nanog and PI3K/Akt signaling in spheroid-forming cells and CD133(+) cells from these cell lines. Our reliance on CD133 as a marker of CSCs is based on several studies from our lab and others showing that this molecule plays a role in the growth and development of tumors including sarcomas^21,37. CD133(+) cells are enriched in CSCs and show greater tumorigenic potential than CD133()- cells in multiple cancers^38–41.

Multidrug chemotherapy with agents such as doxorubicin, ifosfamide, gemcitabine, and docetaxel is standard treatment for patients with advanced or metastatic sarcomas. These drugs can lead to tumor shrinkage but resistance ultimately develops. Our results implicate Nanog in the resistance of sarcoma CSCs to chemotherapy and radiation; we found that Nanog in spheroid-forming cells reduced chemo- and radiotherapy resistance, increased apoptosis, and attenuated the tumor growth of flank xenografts. These data are in line with extensive evidence supporting Nanog’s vital role in malignant disease; its expression correlates with cell proliferation, tumorigenicity, and invasiveness^42–44.

Our phospho-kinase array analysis revealed that Akt1/2 is more highly activated in CD133(+) vs. CD133(−) sarcoma cells and spheroid vs. monolayer sarcoma cells. This finding is in agreement with prior reports that the Akt pathway contributes to the self-renewal and maintenance of CSCs^25,45, and with the central role of Akt activation in sarcomagenesis^46–49. The key advance in our study is that we show that Akt signaling supports the maintenance of sarcoma CSC phenotypes such as self-renewal⁵⁰, and chemo- or radiotherapy resistance and its activation in human sarcomas, as well as the correlation of that activation with expression of CD133 and Nanog. These findings demonstrate that Akt signaling contributes to the control of expression of CSC transcription factors in human sarcoma. Our results support targeting the Akt pathway to prevent resistance to chemotherapy and radiotherapy and increase the likelihood of durable remission, as has been suggested for many cancers⁴⁰, including several sarcomas^49,51–55.

In conclusion, our findings indicate that Akt1/2–Nanog signaling plays a critical role in sarcoma CSC maintenance. Thus, targeting the Akt1/2–Nanog signaling pathway may prevent or reverse CSC phenotypes, tumor progression, and radiotherapy resistance in sarcomas.

Materials and methods

Cell lines and reagents

HT1080 human fibrosarcoma cells and SK-LMS-1 human leiomyosarcoma cells were obtained from the American Type Culture Collection (ATCC, Manassas, VA). The DDLS8817 dedifferentiated liposarcoma cell line was established from a patient sample following informed consent and were confirmed by cytogenetic analysis and by DNA copy number arrays (Agilent 244K) to harbor chromosome 12q amplification. HT1080 and SK-LMS-1 cells were maintained in Dulbecco’s modified Eagle’s medium (DMEM), and DDLS8817 cells were maintained in DMEM-F12. All media were supplemented with 10% fetal bovine serum (FBS), penicillin (100 U/mL), streptomycin (100 μg/mL), and l-glutamine (2 mM) (hereafter termed “regular media”). Cancer cell lines were actively passaged for less than 6 months from the time that they were received, following United Kingdom Coordinating Committee on Cancer Research guidelines⁵⁶. Doxorubicin (RYG02) was purchased from Biotang Inc. (Lexington, MA). LY294002 (cat. 440202) and Puromycin (cat. 508838) were purchased from Calbiochem.

Spheroid generation

Cells were resuspended in spheroid media, comprised of DMEM/F12 containing epidermal growth factor (EGF, E9644; Sigma-Aldrich, St. Louis, MO), basic fibroblast growth factor (bFGF, 341583; Sigma-Aldrich), N-2 supplement (A13707-01; Thermo Fisher Scientific, Waltham, MA), and B27 (0080085SA; Sigma-Aldrich), and then plated on Ultra-Low Attachment culture dishes (Corning Life Sciences, Tewksbury, MA). Spheroids were collected after 5–7 days except when noted otherwise. Proteins were extracted for analysis, or cells were dissociated with Accutase (561527, BD Biosciences) and used for other experiments. Spheroid growth was quantified as the average number of spheroids >50–100 μm in diameter among five fields after image processing using Imaris 7.6 (Bitplane, Concord, MA).

Single-cell spheroid growth assay

Spheroids were treated with LY294002 (10 μM) or DMSO, dissociated into single cells, and plated onto Ultra-Low Attachment 96-well plates at a density of 1 cell per well. Clone formation was monitored at 1, 4, 7, and 10 days on an inverted microscope (Leica Microsystems, Buffalo Grove, IL). Clone size was measured using MetaMorph software, version 7.8.2 (Molecular Devices, Sunnyvale, CA). Data reflect the mean of three samples.

Western blot analysis

Proteins were extracted by collecting cells in RIPA buffer (Sigma-Aldrich) containing Complete Protease Inhibitor Cocktail (Roche, Indianapolis, IN), and protein concentration was determined using the Bio-Rad Protein Assay (Bio-Rad, Hercules, CA). Proteins were detected using the following antibodies: CD133 (MBS462020) from MyBioSource (San Diego, CA); Sox2 (#2748), Oct4 (#2788), Nanog (#4893), p-Akt (T308) (#9275), p-AKT(Ser 473) (#9271), p-Erk1/2 (#9101), cleaved caspase-3 (#96610, all from Cell Signaling Technology; c-Myc (sc-40), Akt1/2 (sc-8312), all from Santa Cruz Biotechnology, Bcl-2 (ab692), both from Abcam), γ-H2AX (05-636; Millipore), and β-actin (A5441; Sigma).

FACS and magnetic-activated cell sorting

For FACS, cells were dissociated using Accutase and resuspended in PBS containing 0.5% BSA. The cells were stained with PE-conjugated CD133 (BD566593) or isotype control antibody (BD555742) from BD Biosciences on ice for 30 min. Cells were then washed with PBS and analyzed on a BD FACSCalibur (BD Biosciences) using Cell Quest software.

CD133+ cells were sorted by a magnetic-activated cell sorting system (Miltenyi Biotech). After collecting spheroids, cells were washed with PBS, dissociated to single cells using Accutase, and stained with CD133-Micro Beads on ice for 30 min. Cells were then passed through an LS magnetic column, where CD133+ cells were retained. The CD133+ cells were then eluted from the column after removal from the magnet. Quantitative analysis of CD133+ cells was performed by immunofluorescence using PE-conjugated CD133 antibody.

Lentiviral transduction

Nanog and Akt1/2 expression was silenced via lentiviral transduction of human Nanog shRNA (sc-43958-V; Santa Cruz) and human Akt1/2 shRNA (sc-43609-V; Santa Cruz) per the manufacturer’s protocol. Nanog was overexpressed via Nanog lentiviral activation particles (sc-418033-LAC; Santa Cruz) per the manufacturer’s protocol. Controls were scramble shRNA control (sc-108080; Santa Cruz) or control Lentiviral Activation Particles (sc-437282, Santa Cruz). Maximal knockdown of genes occurred 72–96 h after transduction.

Cell proliferation

Spheroids were dissociated with Accutase, and monolayer cells were collected following detachment using trypsin. For proliferation assays, 2 ×103 cells were plated onto 96-well flat-bottom plates and maintained in regular media overnight. After 1 day, cells were treated with doxorubicin (1.5 μg/mL) or radiation (6 Gy). A colorimetric MTT assay was used to assess cell number by optical density after 5 days or the specified number of days, as previously described⁵⁷. Data reflect the mean of 6 samples.

NANOG and CD133 mutation and copy number alteration analysis from various databases

To determine the frequency of CD133 and Nanog mutations and copy number alterations (amplifications and deletions) in sarcoma samples from previous genomic studies, we selected sarcoma samples from TCGA³¹, Liu et al.³², other groups³³ and Memorial Sloan Kettering Cancer Center (https://cbioportal.mskcc.org/), along with types of alterations in cBioPortal (http://www.cbioportal.org) and http://cancergenome.nih.gov. Progression-free survival data were available for these patients. Kaplan–Meier estimates were used to generate progression-free survival plots. The log-rank test was used to compare survival outcomes.

Comet assay

HT1080 and SK-LMS-1 cells were transduced with Nanog shRNA or control scrambled shRNA and grown as spheroids. Some spheroids with treated with 6 Gy of radiation. After 24 h, spheroids were dissociated into single cells. The single-cell gel electrophoresis assay, also known as the comet assay, was carried out using Comet Assay Kit (Trevigen Inc., Gaithersburg, MD, USA) per the manufacturer’s instructions. After electrophoresis, the slides were stained with 20 μL of 1 μg/mL DAPI and analyzed with a fluorescence microscope. Bleomycin was not added. Olive tail moment values (equal to the product of the tail length and the fraction of total DNA in the tail) were calculated from at least 50 cells for each group using Komet 5.5 software (Andor Technology, Belfast, UK).

Immunocytochemistry

Spheroid cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100 in PBS. Following cell fixation, cells were incubated with antibodies recognizing CD133 (MBS462020; MyBioSource), Nanog (#4893; Cell Signaling), and γ-H2AX (05-636; Millipore) in a solution of PBS with 1% FBS and 0.1% Triton X-100 at 4 °C overnight. Cells were then stained with secondary antibodies tagged with Alexa Fluor 488 (A-11029) or Alexa Fluor 568 (A-11061), both from Thermo Fisher. Nuclei were counterstained using 4′,6-diamidino-2-phenylindole (DAPI, 28718-90-3; Sigma-Aldrich). Stained cells were visualized on an inverted confocal microscope (Leica Microsystems) and images were processed using Imaris version 7.6 (Bitplane). Three samples were examined for each group, and each sample was visualized for five fields.

Human phospho-kinase array

Phospho-antibody array analysis was performed using the Proteome Profiler Kit ARY003B (R&D Systems). The array membranes were incubated with 500 µg lysate overnight at 4 °C. The following day, chemiluminescent detection was done according to the manufacturer’s protocols²⁴. Densitometry analysis was performed using ImageJ.

Mouse xenograft model

All mouse protocols were approved by the Institutional Animal Care and Use Committee. To generate subcutaneous flank tumors, 2 × 10⁶ HT1080 cells (following shRNA knockdown of Nanog or Akt1/2 where indicated) were resuspended in 100 μL of Hank’s balanced salt solution (HBSS) and injected subcutaneously into the right flank of athymic 6–8-week-old male BALB/c nu/nu mice (Taconic, Hudson, NY) following isoflurane anesthesia. Mice were randomly assigned by coin flip into treatment groups (6 mice per group) when tumors reached 100–150 mm³ in volume. The investigator was not blinded. Sample size was determined using the sample a size program (http://hedwig.mgh.harvard.edu/sample_size/size.html). Doxorubicin (4 mg/kg) or PBS was administered two times per week by intraperitoneal injection or as indicated. Tumor volume was calculated using the formula length × (width)² × 0.52. To radiate tumors, mice were anesthetized using ketamine (125 mg/kg) and xylazine (10 mg/kg), placed in shielded device to expose only the flank tumor, and irradiated using a Gammacell 40 Exactor Irradiator (Best Theratronics, Ottawa, ON, Canada).

Immunohistochemistry of xenograft tumors

At least four sections were analyzed from each tumor. Paraffin-embedded sections were deparaffinized⁵¹, and then incubated with one or more of the following primary antibodies recognizing Sox2 (ab93689), Oct4 (ab18976), Nanog (ab80892), c-Myc (ab125275; Abcam), Ki67 (ab15580) (all from Abcam), cleaved caspase-3 (#9661; Cell Signaling), Bcl-2 (Santa Cruz, sc-65392), or CD133 (MBS462020; MyBioSource) in a solution of PBS with 1% FBS and 0.1% Triton X-100 at 4 °C overnight. Staining was visualized using secondary antibodies tagged with Alexa Fluor 488 (A-21206) or Alexa Fluor 568 (A-11011), both from Thermo Fisher. Nuclei were counterstained using DAPI. Slides were digitally scanned with Panoramic Flash 250 (3DHistech, Budapest, Hungary) using a ×20/0.8 NA objective, and stained cells were counted in five microscopic fields. Images were processed using MetaMorph version 7.8.2 (Molecular Devices).

Tumor microarray

Commercially available paraffin-embedded tissue array slides containing 79 human sarcomas and 4 human normal tissues (NBP2-30332; Novus Biologicals, and T242, US Biomax, Inc., USA) were purchased. Sections were deparaffinized, then incubated with antibodies recognizing human CD133 (MBS462020; MyBioSource), Nanog (ab80892; Abcam), and p-Akt1/2 (#9271; Cell Signaling) in a solution of PBS with 1% BSA and 0.1% Triton X-100 at 4 °C overnight. Staining was visualized using secondary antibodies tagged with Alexa Fluor 488 (A32766, A10042) and Alexa Fluor 594 (A32744, A32754), from Thermo Fisher, with nuclear counterstaining using DAPI. Images were collected on an inverted confocal microscope (Leica Microsystems) and processed using Imaris 7.6. Five fields were examined for each sample.

Statistical analysis

Statistical analyses were performed using Microsoft Office Excel 2010. P values were calculated using Student’s t-test. For comparisons between more than two groups, treatment groups were compared to the control using one-way ANOVA with the Bonferroni adjustment for multiple comparisons. Variance was assumed to similar between groups. All experiments were repeated independently at least twice. P values < 0.05 were considered significant. Sample sizes were using a sample size program (http://hedwig.mgh.harvard.edu/sample_size/size.html).

Conflict of interest

The authors declare that they have no conflict of interest.

Supplementary information

Supplementary Information accompanies this paper at (10.1038/s41389-020-00300-z).