Cancer Stem Cells: Targets for Cancer Therapy

The Cancer Stem Cell Hypothesis

Are stem cells involved in cancer? Cancer stem cells (CSC’s) are subpopulations of cancer cells that can self-renew, generate diverse cells in the tumor mass, and sustain tumorigenesis¹. Cancer researchers hypothesizes that tumors arises from CSCs that originate as a result of mutational hits on normal stem cells, by the transformation of restricted progenitor cells or even the differentiated cells that acquire self-renewing capacity². These CSCs drive tumor progression and recurrence after chemotherapy treatments and have recently become targets for cancer stem cell therapies³. Since both normal stem cells and cancer cells possess ability to self-renew, many pathways that are classically associated with cancer are also involved in the regulation of normal stem cell development including Notch, Wnt, Shh and classical pluripotency transcription factor pathways Oct-4, Sox-2 and Nanog⁴.

An Illustration of the Cancer Stem Cell Hypothesis

3D Spheroid Culture of CSC

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Cancer stem cells (CSCs) seek out a niche created within the tumor 3D microenvironment⁵. A miniscule number of cells within an in vitro 3D tumor spheroid or an in vivo tumor exhibit “stem cell-like” characteristics including 1) slowed proliferation rate 2) self-renewal capabilities and 3) undifferentiated phenotype that can undergo multilineage differentiation. CSCs, which can reconstitute tumors following drug treatment, have been described in both 3D spheroid models and in patients undergoing chemotherapy⁶. Increased expression of “stemness-related genes” was observed when comparing solid tumor cell lines grown as 3D spheroids to monolayers⁷. While clearly not definitive proof of the presence of CSCs, these types of results illustrate the tendency for the in vitro 3D microenvironment to create a “stem cell-like” population similar to the in vivo population believed to be responsible for tumor drug resistance.

Cancer Stem Cell Media

Traditionally, CSCs have been isolated and grown from cancer cell lines and tumor biopsies in undefined serum containing media using 3D tumorsphere aggregates. However, using undefined culture conditions has led to experimental variability and suboptimal cell growth. 3dGRO™ Spheroid Medium is a new chemically defined and serum-free CSCs media that supports the expansion of CSC’s in 3D tumorsphere cell cultures. The media supports serial passaging of cancer cell lines as tumorspheres leading to an overall enrichment of CSC population overtime.

Features and Benefits

• Chemically defined, Serum-free formulation.
• High tumorsphere formation efficiency.
• Allows extended serial tumorsphere passaging (>10).
• Proven to enrich CSCs from numerous cancer cell lines.

Cell Lines tested with 3dGRO™ Spheroid Medium

MCF-7, A-431, Panc-1, LNCaP, HT-29, A-549, U-87 MG, HT1080, E006AA

Figure 1. 3D Tumorsphere formation of MCF7 breast cancer and E006AA prostate cancer cells at Passage 5 cultured in 3dGRO™ Spheroid Medium.

3D Spheroid Formation Plates

Corning^® Costar^® Ultra-Low attachment multi-well plates are designed to inhibit cell attachment to efficiently form 3D spheroids, including cancer stem cells. The surface is coated with a highly hydrophilic and neutrally charged coating that binds to polystyrene forcing seeded cells into a suspended floating state. The coating is stable, nontoxic, biologically inert and non-degradable.

Cancer Stem Cell Markers

Small populations of stem-like cells have been isolated from most leukemias as well as from many solid tumors such as brain glioblastomas, medulloblastomas, breast, cervical, colorectal, gastrointestinal, hepatocellular, lung, pancreatic, prostate, and skin carcinomas⁸. Cancer stem cells display the same cell surface markers as their normal counterparts, but demonstrate uncontrolled proliferation, perhaps due to a reduced responsiveness to negative growth regulators or to the loss of contact inhibition and gap junction intercellular communication (GJIC).

Table 1. Cancer Stem Cell Markers

Markers	Normal Stem Cells	Cancer Stem Cells
Oct3/4, Sox2, Nanog	Maintenance of pluripotency and self-renewal of ES and iPS cells	Highly expressed in poorly differentiated tumors of breast cancer, glioblastomas and bladder cancers. Up regulation of transcription factors in stem-like cells
CD133 (Prominin-1)	Marker for hematopoietic stem cells, neural stem cells and somatic stem cells found in many tissues	Higher clongenicity, invasiveness and tumorigenesis in human oral squamous cell carcinomas.
CD44	Self-renewal and differentiation	Up-regulation in solid tumors and HNSCC cancers
ALDH	Stem like properties including colony formation, self-renewal and tumorigenesis	Marker for normal and malignant mammary stem cells. Prognostic marker for breast cancer and predictor of metastasis.
Side Populations (Hoechst)	Enriched in hematopoietic stem cells	Identified in solid tumors such as hepatocellular carcinoma, glioma, ovarian and breast cancers

Table 2. Cancer Stem Cell Antibodies

CD133

CD44

CD24

CD29

CD90

Nestin

SCA-1

BMI-1

ALDH1

OCT3/4

Cancer Stem Cell ALDH Detection

CSCs are unique as they express elevated levels of aldehyde dehydrogenase (ALDH) ⁹. Historically, the ALDEFLUOR™ assay has been used to measure ALDH levels and has been influential to study rare CSCs populations. The ALDEFLUOR assay emits in the green region of the electromagnetic spectrum (512 nm). Thus, the reagent cannot be simultaneously utilized in cells or mice expressing green-fluorescent proteins emitting in the green fluorescent spectrum. AldeRed is a red-shifted fluorescent substrate for ALDH used for labelling viable ALDH positive cells leaving the green emission channel available for further experimentation¹⁰. The AldeRed ALDH Detection Assay addresses current limitations of the ALDEFLUOR assay.

AldeRed Features and Benefits:

• Red-shifted assay leaves green channel available for further experimentation
• Live stem cell identification enables flow sorting of rare cell populations
• Rapid enzymatic assay protocol

Figure 2. AldeRed 588-A is a fluorescent and non-toxic ALDH substrate that diffuses freely into live intact and viable cells, but remains trapped inside the cells once converted by ALDH into the corresponding acid.

References

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2. Adams P, Jasper H, Rudolph K. 2015. Aging-Induced Stem Cell Mutations as Drivers for Disease and Cancer. Cell Stem Cell. 16(6):601-612. https://doi.org/10.1016/j.stem.2015.05.002

3. Vinogradov S, Wei X. 2012. Cancer stem cells and drug resistance: the potential of nanomedicine. Nanomedicine. 7(4):597-615. https://doi.org/10.2217/nnm.12.22

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5. Plaks V, Kong N, Werb Z. 2015. The Cancer Stem Cell Niche: How Essential Is the Niche in Regulating Stemness of Tumor Cells?. Cell Stem Cell. 16(3):225-238. https://doi.org/10.1016/j.stem.2015.02.015

6. Vidal SJ, Rodriguez-Bravo V, Galsky M, Cordon-Cardo C, Domingo-Domenech J. 2014. Targeting cancer stem cells to suppress acquired chemotherapy resistance. Oncogene. 33(36):4451-4463. https://doi.org/10.1038/onc.2013.411

7. Wong DJ, Segal E, Chang HY. 2008. Stemness, cancer, and cancer stem cells. Cell Cycle. 7(23):3622-3624. https://doi.org/10.4161/cc.7.23.7104

8. Nguyen LV, Vanner R, Dirks P, Eaves CJ. 2012. Cancer stem cells: an evolving concept. Nat Rev Cancer. 12(2):133-143. https://doi.org/10.1038/nrc3184

9. Marcato P, Dean CA, Giacomantonio CA, Lee PW. 2011. Aldehyde dehydrogenase: Its role as a cancer stem cell marker comes down to the specific isoform. Cell Cycle. 10(9):1378-1384. https://doi.org/10.4161/cc.10.9.15486

10. Minn I, Wang H, Mease RC, Byun Y, Yang X, Wang J, Leach SD, Pomper MG. 2014. A red-shifted fluorescent substrate for aldehyde dehydrogenase. Nat Commun. 5(1): https://doi.org/10.1038/ncomms4662