August 6, 2014


Background: Stem cells are attractive candidates for the development of novel therapies, targeting indications that involve functional restoration of defective tissue. Although most stem cell therapies are new and highly experimental, there are clinics around the world that exploit vulnerable patients with the hope of offering supposed stem cell therapies, many of which operate without credible scientific merit, oversight, or other patient protection.

Methods: The authors review the potential and the drawbacks of incorporation of stem cells in cosmetic procedures. A review of U.S. Food and Drug Administration–approved indications and ongoing clinical trials with adipose stem cells is provided. Furthermore, a “snapshot” analysis of Web sites using the search terms “stem cell therapy” or “stem cell treatment” or “stem cell facelift” was performed.

Results: Despite the protective net cast by regulatory agencies such as the U.S. Food and Drug Administration and professional societies such as the American Society of Plastic Surgeons, the authors are witnessing worrying advertisements for procedures such as stem cell face lifts, stem cell breast augmentations, and even stem cell vaginal rejuvenation. The marketing and promotion of stem cell procedures in aesthetic surgery is not adequately supported by clinical evidence in the majority of cases.

Conclusions: Stem cells offer tremendous potential, but the marketplace is saturated with unsubstantiated and sometimes fraudulent claims that may place patients at risk. With plastic surgeons at the forefront of stem cell–based regenerative medicine, it is critically important that they provide an example of a rigorous approach to research, data collection, and advertising of stem cell therapies.

Cosmetic surgery is a lucrative business, with $11 billion spent on cosmetic procedures in the United States in 2012.1 Over the past decade, the demand for cosmetic procedures has increased. This is likely attributable to a combination of an aging population, a desire to retain youthful appearance, growing social acceptance of cosmetic procedures, and the availability of minimally invasive options. According to the American Society of Plastic Surgeons 2012 report, the number of cosmetic procedures performed by its members over the previous year was 14.6 million, up 5 percent from 2011.1 Interestingly, there has been an increase in the number of minimally invasive procedures and a decrease in the number of surgical procedures being performed.1 Facial procedures saw the most growth in 2012.1

A shift toward more minimally invasive techniques has resulted in a wider range of practitioners performing cosmetic procedures.2 Along with plastic surgeons, these include dermatologists, family medicine practitioners, anesthesiologists, and ophthalmologists.3 A worrying trend is the rise in the number of non–surgery-trained individuals providing surgical cosmetic treatments, especially liposuction.4 This trend has challenged the traditional practice of plastic surgery and resulted in the emergence of a corporate medicine model, where the public is bombarded with the promotion of trademarked procedures/devices and advertising that promises stunning results, with claims of innovation, superiority, and improved safety.5 Operations that once included detailed history and physical examinations, along with lengthy consultations, are being threatened by the commoditization of cosmetic procedures, with salespeople who tell prospective patients what “work” they need done.6

Another worrying aspect of unregulated stem cell clinics is that practitioners, ranging in expertise from plastic surgeons to obstetricians, along with other specialists are treating conditions that they would not encounter in their normal clinical practice, such as Parkinson’s disease. This is an unrealistic and potentially dangerous use of adult stem cells. Although the potential of adipose-derived stromal cells to differentiate into neurons has been established in vitro and in a few in vivo studies, there is still insufficient evidence to justify their use clinically.7 Spontaneous differentiation of adipose-derived stromal cells into therapeutic cell types for Parkinson’s disease is biologically unrealistic.8 Injecting immature stem cells does not provide a long-term treatment for Parkinson’s disease, and the risk associated with uncontrolled growth of transplanted cells is unacceptable.8

In line with this recent shift in marketing practice has been the emergence of stem cell–related therapies. Although stem cell therapy remains in its infancy, there are a growing number of cosmetic practitioners that are advertising minimally invasive, stem cell–based rejuvenation procedures. With unsubstantiated claims that these procedures are safer, have equivalent or better outcomes, and have faster recovery periods than conventional procedures, many of these practitioners are emphasizing profit over quality and safety. Importantly, the emergence of innovative advances in cell-based therapies requires the same rigor in experimental testing that is required for all other medical therapies to ensure the safety and education of our patients.

Back to Top | Article Outline


Stem cells have captured the imagination of many because of deeper insights into the biology of cells they provide and the potential for treatment of many diseases. Stem cells are functionally defined by their ability to self-renew and to generate differentiated progeny cells with more restricted potential.9 The role of stem cells changes significantly throughout life, as stem cells must alter their properties to match the changing growth and regeneration demands. Reflecting these changing roles, there are many different types of stem cells that have been defined. Pluripotent stem cells, such as embryonic or induced pluripotent stem cells, have the capacity to generate tissue from any of the three germ layers.10,11 Their clinical use, however, has been hampered by risks for teratoma formation and, in the case of embryonic stem cells, ethical concerns.12 Multipotent stem cells, such as mesenchymal stromal cells, lack these shortcomings but have the capacity to differentiate into a more limited number of closely related cells.13,14 Finally, unipotent stem cells, although retaining the ability to self-renew, can produce only one cell type. This last class, although having limited utility in regenerative strategies, is intimately involved in normal tissue homeostasis at a wide variety of sites, including skin, lung, liver, and intestinal lining.15–18

Of these different types of stem cells, of particular clinical interest are the mesenchymal stromal cells. Mesenchymal stromal cells have the capacity to differentiate into bone, cartilage, muscle, and fat. Although the best-characterized mesenchymal stromal cells are the bone marrow–derived mesenchymal stromal cells, their clinical utility is limited, as isolation of these cells is associated with considerable donor-site morbidity and low yield. However, Zuk and colleagues identified a similar cell type with greater ease of harvest and higher yield in mature adipose tissue that also possessed multilineage potential.13 Importantly, the stromal vascular fraction from which these adipose-derived stromal cells are derived is highly heterogeneous, and also contains an array of other cell types including endothelial cells, pericytes, fibroblast, leukocytes, hematopoietic stem cells, and endothelial progenitor cells.19 Although a comprehensive profile of antigen expression has yet to be established for adipose-derived stromal cells, studies have characterized these cells within the stromal vascular fraction by the following antigen profile: CD45, CD235a, CD31, CD34+, CD106, and CD36+.20 In general, their abundance and relative ease of harvest along with their autogenous immune-privileged status as a result of human leukocyte antigen-DR expression have made them into an attractive candidate for regenerative therapies.21

The most notable area of aesthetic surgery where adipose-derived stromal cells may be applicable is autologous fat grafting. Autologous fat grafting has become popular for soft-tissue augmentation throughout the entire body.22,23 However, there is much variability in the literature regarding the high resorption of fat grafts.24 These disappointing and unpredictable outcome data provided the impetus for developing strategies for improving fat graft survival. One such strategy is cell-assisted lipotransfer where the stromal vascular fraction containing adipose-derived stromal cells is isolated from a portion of the aspirated fat and then recombined with the remaining fat before injection.25 Interestingly, Yoshimura and colleagues reported that they were able to achieve stable augmentation of 100 to 200 ml using cell-assisted lipotransfer after a mean fat injection of 270 ml in patients undergoing cosmetic breast augmentation.25 Similarly, enrichment of fat grafts with adipose-derived stromal cells was also reported to enhance volume retention following injection into the upper arm.26 This strategy, however, remains controversial, as a comparative clinical study reported no significant difference in fat graft retention between cell-assisted lipotransfer and water-assisted lipotransfer for breast augmentation.27 Although holding tremendous promise, the clinical use of adipose-derived stromal cells in aesthetic surgery is thus still in its infancy. It is therefore vital that clinical practice should be guided by critical evaluation of the data, ideally in level I evidence studies, rather than anecdotes, word of mouth, or attention-grabbing headlines.

As has been noted previously by colleagues in the plastic surgery community, it is also vitally important to use appropriate terminology and take care not to confuse traditional autologous fat grafting with therapies that specifically use adipose-derived stromal cells.28 To avoid misleading the public, it will be important to distinguish between simple soft-tissue volumetric augmentation of the face using standard fat grafting versus fat grafts enriched with adipose-derived stromal cells. It is also important not to use potentially confusing terminology such “stem cell face lift” to describe procedures that are nothing more than volumetric lipofilling with or without adipose-derived stromal cell enrichment.29

With every new scientific advancement, it is the responsibility of scientists and physicians to guide and educate the public on the advantages and disadvantages of any proposed therapy. Overstating potential benefits based on early and incomplete evidence can only serve to erode the public’s trust in the medical profession and, more concerning, compromise the safety of our patients. For example, there is still some uncertainty in the literature regarding the ability of adipose-derived stromal cells to generate certain lineages in vivo.30Furthermore, there have been conflicting reports in the literature regarding the potential for adipose-derived stromal cells to promote or inhibit tumorigenesis.31–36 Further areas of concern regarding adipose-derived stromal cells in aesthetic surgery relate to the possible use of nonautologous cells in countries outside of the United States. These cells should be used in an autologous fashion to minimize any immunologic consequences as a result of self-identity/non–self-identity. Finally, the use of stem cells in aesthetic procedures, not unlike other nonaesthetic indications, opens up the possibility of medical tourism and misrepresenting therapeutic benefits to attract patients.

Nevertheless, it is clear that adipose-derived stromal cells have the potential to play an important role in both regenerative medicine and cosmetic surgery. Gir et al. reported that, by 2012, of the 174 published cases of patients treated with adipose-derived stromal cells and 121 patients enrolled in clinical trials in the plastic surgery literature, no major adverse effects were noted.37 Although encouraging, it is essential that plastic surgeons proceed with caution and only after close scrutiny of the hard evidence. Standard protocols for the use of these cells must still be developed, such as optimal numbers of adipose-derived stromal cells to be used per treatment. To that end, the American Society of Plastic Surgeons and the American Society for Aesthetic Plastic Surgery have commissioned task forces to develop position statements built on the best available data.38These attempts to provide a unified and coherent approach based on up-to-date data must be commended.

Back to Top | Article Outline


Because of the potential for stem cells and the burgeoning interest for incorporation of these cells into various cosmetic procedures, we characterized the direct-to-consumer marketing of stem cell medicine through a content analysis of corporate Web sites obtained by a Google search ( using the search terms “stem cell therapy” or “stem cell treatment” or “stem cell facelift” in November of 2013. This “snapshot” of 50 cosmetic clinics offering “stem cell” treatment reflects the current state of marketing and is analyzed inFigures 1 and 2. The use of the “stem cell” label was taken at face value, and despite adopting this approach in the following analysis, we have no knowledge of the true quality of stem cells used. Because of the heterogeneity of isolated cell populations, particularly in fat, and an inability of these practitioners to sort the cells by flow or magnetic cytometry, it is likely that the cells used by these clinics, as elaborated above, contain a host of other cells in addition to fat-derived stromal cells.

Fig. 1
Fig. 1
Image Tools
Fig. 2
Fig. 2
Image Tools

In addition, numerous clinics were found to offer platelet-rich plasma treatments that they marketed as stem cell treatment. Of note, platelet-rich plasma does not contain stem cells and is instead autologous plasma that is enriched with platelets.39 Indeed, platelets by their very nature are cell fragments and technically do not even come under the umbrella term of cells, as they lack a cell nucleus. Nonetheless, platelet-rich plasma has found application in a range of clinical scenarios such as orthopedics, ophthalmology, and wound healing, serving as a growth factor pool for improving tissue regeneration.40 However, to market platelet-rich plasma as a stem cell therapy is misleading.

Back to Top | Article Outline


As use of stem cells in cosmetic medicine continues to expand, it is important to note that U.S. Food and Drug Administration approval remains limited. In June of 2011, after almost 10 years of review, the U.S. Food and Drug Administration approved azficel-T (laViv; Fibrocell Science, Inc., Exton, Pa.), a first-in-class personalized cell therapy for eliminating fine wrinkles or nasolabial folds around the nose and mouth.41 Each laViv treatment involves harvesting a patient’s own fibroblasts from behind the ear, culturing them for 90 days, and then reinjecting expanded cells into the dermis during a series of treatments.41 The company’s safety data were sufficient to warrant approval, but because laViv is so novel, approval was contingent on extensive postmarket surveillance for immune effects and skin cancer.41

A search for “adipose stem cells” on the Web site yielded 109 results. However, only a small proportion of these clinical trials focus on cosmetic treatments. Studies that do focus on cosmetic procedures include trials to establish the role of adipose-derived stromal cells in volume retention of fat grafts, improving fat graft retention in the breast following breast cancer resection, reducing wrinkles when co-delivered with fat grafts, skin ulcers, diabetic wounds, and improving skin quality of irradiated breasts. In addition, one study is presently looking at the role of adipose-derived stromal cells to improve osteogenesis in composite tissue grafts and another is looking at the role of adipose-derived stromal cell–enhanced fat grafts following craniofacial trauma.

Back to Top | Article Outline


When considering clinical use of stem cells, one must be cognizant of the fact that cell and tissue processing pose a risk of contamination and/or damage to cells. Regulation of stem cell therapy is thus essential to ensure patient safety. For this reason, the growing number of “stem cell–based” cosmetic procedures is worrisome, because of the lack of oversight and dearth of scientific studies or trials to evaluate their efficacy and safety in vivo.

Potential contamination of and damage to cells becomes an issue when cell-based products involve more than minimal manipulation, including cell expansion in culture and differentiation.42 In theory, cells removed from a patient and replaced during the same surgical procedure pose no greater risk of disease transmission than the operation itself.42 However, cell culture typically involves the use of nonhuman serum, usually obtained from fetal calves, and therefore introduces a potential risk for prion infection.43 In light of this, current U.S. Food and Drug Administration guidelines specify that fetal calf serum must come from a country certified to be free of this disease. In addition, cell expansion in vitro may also involve the use of xenogenic feeder cells, particularly in the case of human embryonic stem cells. This also poses a potential risk of infectious disease transmission.

Another safety concern revolves around malignant stem cell transformation. Stem cells have clear similarities to cancer stem cells, and it has been demonstrated that mesenchymal stromal cells can undergo spontaneous malignant transformation following long-term in vitro culture.44 Despite the enormous potential for stem cells demonstrated in preclinical testing, it is essential to recognize and appreciate both the promise and limitations for use of stem cells in clinical therapeutics.45

Back to Top | Article Outline


Antiaging therapies seek to delay degeneration of the skin and its support system. As aging proceeds, reduced skin elasticity secondary to changes in skin thickness and collagen organization and solar elastosis results in skin folds and wrinkles.46,47 Extrinsic effects such as photoaging also contribute significantly to changes in skin aesthetics through the induction of irregular pigmentation, dyschromia, and wrinkles.46,48 It is important to bear in mind that the mechanisms behind aging are cellular and molecular in nature, and therefore any therapy claiming to have antiaging effects must directly impact these mechanisms. In this regard, although volumetric enhancement often results in a more youthful form and appearance, it does not represent a true antiaging therapy for this reason.

Collagen remodeling represents an effective target for antiaging therapies. Laser treatment can induce collagen remodeling by promoting synthesis of both type I and type III collagen.49,50 In addition to laser treatment, cytokines and growth factors can impact collagen remodeling through their effects on dermal fibroblasts. Given the ability of cytokines such as vascular endothelial growth factor, platelet-derived growth factor, and transforming growth factor-β to promote collagen synthesis and turnover, stem cells capable of producing these factors may hold promise for antiaging therapies. The ability of adipose-derived stromal cells to produce an array of cytokines therefore makes them a candidate for antiaging therapies. However, the evidence to support the antiaging effects of stem cells remains minimal at best.

Relatively few studies on adipose-derived stromal cells and other stem cells have demonstrated what could be considered a true antiaging effect. One such study claimed that adipose-derived stromal cells minimized the appearance of ultraviolet B–induced wrinkles in mice through the activation of dermal fibroblasts by secreted factors.51 More often than not, however, improved facial and skin aesthetics is achieved through enhanced volumetric rejuvenation by transplanted cells. Rather than a true stem cell face lift, where transplanted cells exert prolonged antiaging effects, these procedures amount to stem cell–enriched lipofilling, a well-known and established technique.

Such criticism is not meant to minimize the efficacy of such therapies for creating a more youthful appearance. There is certainly room for improvement within the field of volumetric rejuvenation, and biomaterials/molecules designed to provide an optimal environment for transplanted stem cells have recently emerged as a promising area of research. For example, autologous mesenchymal stromal cells when combined with hyaluronic acid were able to fill in deep skin folds in the face, showing progressive improvement of skin tone and decreasing lines of expression.52 Slowing or even reversing the effects of aging thus requires a precise understanding of the molecular and cellular events involved in the aging process, events that may not be fully addressed by volume filling alone.

Back to Top | Article Outline


Another important consideration regarding incorporation of stem cells into cosmetic procedures is the effect of age on the cells themselves. Stem cells are not immune to the process of aging, and their function is tightly regulated by their surrounding environment, known as the stem cell niche. The hematopoietic system provides the best evidence for the role local environment plays in guiding maintenance and differentiation of stem cell populations and the effects of aging on this balance. Studies have shown that hematopoietic stem cells have reduced functional ability as the capacity to give rise to progeny cells becomes skewed toward the myeloid lineage because of transcriptional changes that occur with advanced age.53 Furthermore, aging is also associated with decreased competence of the adaptive immune system and an increased incidence of myeloid diseases, including leukemias.54,55

The functional decline of aged stem cells is caused by a host of factors. These include both exogenous sources, such as genotoxic chemicals, ultraviolet irradiation, and ionizing radiation; and endogenous sources, such as a build-up of reactive oxygen species, telomere attrition, and stalled replication forks.56,57 A series of experiments evaluating hematopoietic stem cell reserves and functional capacity in young and old mice deficient in several different DNA-repair pathways demonstrated the impact of DNA damage on stem cell function.58,59 With age, stem cells were found to accrue DNA damage, and depending on the nature and extent of this damage, mutagenic lesions arising in stem cells have the potential to drive cells to senescence, apoptosis, or tumor transformation.56,58 Therefore, as aging has been associated with a cell-intrinsic decline in the regenerative potential of stem cells, claims of rejuvenation in aged individuals through transfer of cells become more dubious.

Back to Top | Article Outline


Organized plastic surgery has embarked on a strategic initiative to incorporate principles of evidence-based medicine into all aspects of education, publication, training, certification, and practice.60–62Currently, the marketplace is characterized by direct-to-consumer, corporate medicine strategies that are characterized by unsubstantiated and sometimes fraudulent claims that put our patients at risk. With plastic surgeons at the forefront of stem cell–based regenerative medicine, it is critically important that we provide an example of a rigorous approach to research, data collection, and advertising of stem cell therapies. Stem cells offer tremendous potential for cosmetic applications, but we must be vigilant to avoid unscientific claims that may threaten this nascent field.

Back to Top | Article Outline


Geoffrey C. Gurtner, M.D., was supported by National Institutes of Health grant RO1 EB005718, Department of Defense grant W81XWH-08-2-0033, and Department of Defense grant 40109. Derrick C. Wan, M.D., was supported by the American College of Surgeons Franklin H. Martin Faculty Research Fellowship, the Hagey Laboratory for Pediatric Regenerative Medicine, and the Stanford University Child Health Research Institute Faculty Scholar Award. Michael T. Longaker, M.D., M.B.A., was supported by National Institutes of Health grants R01 DE021683-01, RC2 DE020771, and U01 HL09976; the Oak Foundation; and the Hagey Laboratory for Pediatric Regenerative Medicine.

Back to Top | Article Outline


1. American Society of Plastic Surgeons. . 2012 Plastic Surgery Statistics Report. ASPS National Clearinghouse of Plastic Surgery Procedural Statistics Available at: Accessed June 2, 2014.
2. Ahn CS, Davis SA, Dabade TS, et al. Cosmetic procedures performed in the United States: A 16-year analysis Dermatol Surg. 2013;39:1351–1359
3. Housman TS, Hancox JG, Mir MR, et al. What specialties perform the most common outpatient cosmetic procedures in the United States? Dermatol Surg. 2008;34:1–7 discussion 8
4. Paik AM, Hoppe IC, Pastor CJ.. An analysis of leading, lagging, and coincident economic indicators in the United States and its relationship to the volume of plastic surgery procedures performed: An update for 2012 Ann Plast Surg. 2013;71:316–319
5. Swanson E. The commercialization of plastic surgery Aesthet Surg J. 2013;33:1065–1068
6. O’Donnell J. Cosmetic surgery gets cheaper, faster, scarier USA Today. 2011
7. Anghileri E, Marconi S, Pignatelli A, et al. Neuronal differentiation potential of human adipose-derived mesenchymal stem cells Stem Cells Dev. 2008;17:909–916
8. Cyranoski D. Korean deaths spark inquiry Nature. 2010;468:485
9. Weissman IL, Anderson DJ, Gage F.. Stem and progenitor cells: Origins, phenotypes, lineage commitments, and transdifferentiations Ann Rev Cell Dev Biol. 2001;17:387–403
10. Xu C, Inokuma MS, Denham J, et al. Feeder-free growth of undifferentiated human embryonic stem cells. Nat Biotechnol. 2001;19:971–974
11. Sun N, Panetta NJ, Gupta DM, et al. Feeder-free derivation of induced pluripotent stem cells from adult human adipose stem cells. Proc Natl Acad Sci USA. 2009;106:15720–15725
12. Wan DC, Wong VW, Longaker MT. Craniofacial reconstruction with induced pluripotent stem cells. J Craniofac Surg. 2012;23:623–626
13. Zuk PA, Zhu M, Mizuno H, et al. Multilineage cells from human adipose tissue: Implications for cell-based therapies Tissue Eng. 2001;7:211–228
14. Zuk PA, Zhu M, Ashjian P, et al. Human adipose tissue is a source of multipotent stem cells. Mol Biol Cell. 2002;13:4279–4295
15. Kordes C, Häussinger D. Hepatic stem cell niches. J Clin Invest. 2013;123:1874–1880
16. Pellettieri J, Sánchez Alvarado A. Cell turnover and adult tissue homeostasis: From humans to planarians. Annu Rev Genet. 2007;41:83–105
17. Liu S, Zhang H, Duan E.. Epidermal development in mammals: Key regulators, signals from beneath, and stem cells Int J Mol Sci. 2013;14:10869–10895
18. Sinclair K, Yerkovich ST, Chambers DC. Mesenchymal stem cells and the lung. Respirology. 2013;18:397–411
19. Locke M, Windsor J, Dunbar PR. Human adipose-derived stem cells: Isolation, characterization and applications in surgery ANZ J Surg. 2009;79:235–244
20. Bourin P, Bunnell BA, Casteilla L, et al. Stromal cells from the adipose tissue-derived stromal vascular fraction and culture expanded adipose tissue-derived stromal/stem cells: A joint statement of the International Federation for Adipose Therapeutics and Science (IFATS) and the International Society for Cellular Therapy (ISCT). Cytotherapy. 2013;15:641–648
21. Gronthos S, Franklin DM, Leddy HA, et al. Surface protein characterization of human adipose tissue-derived stromal cells. J Cell Physiol. 2001;189:54–63
22. Klein AW, Elson ML.. The history of substances for soft tissue augmentation Dermatol Surg. 2000;26:1096–1105
23. Coleman SR, Saboeiro AP. Fat grafting to the breast revisited: Safety and efficacy. Plast Reconstr Surg. 2007;119:775–785; discussion 786
24. Fisher C, Grahovac TL, Schafer ME, et al. Comparison of harvest and processing techniques for fat grafting and adipose stem cell isolation Plast Reconstr Surg. 2013;132:351–361
25. Yoshimura K, Sato K, Aoi K, et al. Cell-assisted lipotransfer for cosmetic breast augmentation: Supportive use of adipose-derived stem/stromal cells. Aesthetic Plast Surg. 2008;32:48–55; discussion 56–57
26. Kølle SF, Fischer-Nielsen A, Mathiasen AB, et al. Enrichment of autologous fat grafts with ex-vivo expanded adipose tissue-derived stem cells for graft survival: A randomised placebo-controlled trial. Lancet. 2013;382:1113–1120
27. Peltoniemi HH, Salmi A, Miettinen S, et al. Stem cell enrichment does not warrant a higher graft survival in lipofilling of the breast: A prospective comparative study. J Plast Reconstr Aesthet Surg. 2013;66:1494–1503
28. Tabit CJ, Slack GC, Fan K, et al. Fat grafting versus adipose-derived stem cell therapy: Distinguishing indications, techniques, and outcomes Aesthetic Plast Surg. 2012;36:704–713
29. Atiyeh BS, Ibrahim AE, Saad DA.. Stem cell facelift: Between reality and fiction. Aesthet Surg J. 2013;33:334–338
30. Locke M, Feisst V, Dunbar PR. Concise review: Human adipose-derived stem cells: Separating promise from clinical need. Stem Cells. 2011;29:404–411
31. Zimmerlin L, Donnenberg AD, Rubin JP, et al. Regenerative therapy and cancer: In vitro and in vivo studies of the interaction between adipose-derived stem cells and breast cancer cells from clinical isolates Tissue Eng Part A. 2011;17:93–106
32. Prantl L, Muehlberg F, Navone NM, et al. Adipose tissue-derived stem cells promote prostate tumor growth. Prostate. 2010;70:1709–1715
33. Muehlberg FL, Song YH, Krohn A, et al. Tissue-resident stem cells promote breast cancer growth and metastasis. Carcinogenesis. 2009;30:589–597
34. Yu JM, Jun ES, Bae YC, et al. Mesenchymal stem cells derived from human adipose tissues favor tumor cell growth in vivo Stem Cells Dev. 2008;17:463–473
35. Grisendi G, Bussolari R, Cafarelli L, et al. Adipose-derived mesenchymal stem cells as stable source of tumor necrosis factor-related apoptosis-inducing ligand delivery for cancer therapy. Cancer Res. 2010;70:3718–3729
36. Kucerova L, Altanerova V, Matuskova M, et al. Adipose tissue-derived human mesenchymal stem cells mediated prodrug cancer gene therapy Cancer Res. 2007;67:6304–6313
37. Gir P, Oni G, Brown SA, et al. Human adipose stem cells: Current clinical applications. Plast Reconstr Surg. 2012;129:1277–1290
38. . ASAPS/ASPS position statement on stem cells and fat grafting Aesthet Surg J.. 2011;31:716–717
39. Sánchez AR, Sheridan PJ, Kupp LI. Is platelet-rich plasma the perfect enhancement factor? A current review. Int J Oral Maxillofac Implants. 2003;18:93–103
40. Amable PR, Carias RB, Teixeira MV, et al. Platelet-rich plasma preparation for regenerative medicine: Optimization and quantification of cytokines and growth factors. Stem Cell Res Ther. 2013;4:67
41. Schmidt C. FDA approves first cell therapy for wrinkle-free visage Nat Biotechnol.. 2011;29:674–675
42. Halme DG, Kessler DA. FDA regulation of stem-cell-based therapies. N Engl J Med. 2006;355:1730–1735
43. Fekete N, Rojewski MT, Fürst D, et al. GMP-compliant isolation and large-scale expansion of bone marrow-derived MSC. PLoS One. 2012;7:e43255
44. Rubio D, Garcia-Castro J, Martin MC, et al. Spontaneous human adult stem cell transformation Cancer Res. 2005;65:3035–3039
45. Fink DW Jr. FDA regulation of stem cell-based products. Science. 2009;324:1662–1663
46. Kawabata K, Kobayashi M, Kusaka-Kikushima A, et al. A new objective histological scale for studying human photoaged skin Skin Res Technol. 2013;20:155–163
47. Luebberding S, Krueger N, Kerscher M. Mechanical properties of human skin in vivo: A comparative evaluation in 300 men and women Skin Res Technol. 2014;20:127–135
48. Lee JY, Kim YK, Seo JY, et al. Loss of elastic fibers causes skin wrinkles in sun-damaged human skin. J Dermatol Sci. 2008;50:99–107
49. Liu H, Dang Y, Wang Z, et al. Laser induced collagen remodeling: A comparative study in vivo on mouse model. Lasers Surg Med. 2008;40:13–19
50. Orringer JS, Kang S, Johnson TM, et al. Connective tissue remodeling induced by carbon dioxide laser resurfacing of photodamaged human skin Arch Dermatol. 2004;140:1326–1332
51. Kim WS, Park BS, Park SH, et al. Antiwrinkle effect of adipose-derived stem cell: Activation of dermal fibroblast by secretory factors J Dermatol Sci. 2009;53:96–102
52. Claudio-da-Silva C, Baptista LS, Carias RB, et al. Autologous mesenchymal stem cells culture from adipose tissue for treatment of facial rhytids (in Portuguese). Rev Col Bras Cir. 2009;36:288–291
53. Pang WW, Price EA, Sahoo D, et al. Human bone marrow hematopoietic stem cells are increased in frequency and myeloid-biased with age Proc Natl Acad Sci USA. 2011;108:20012–20017
54. Linton PJ, Dorshkind K. Age-related changes in lymphocyte development and function Nat Immunol. 2004;5:133–139
55. Lichtman MA, Rowe JM. The relationship of patient age to the pathobiology of the clonal myeloid diseases Semin Oncol. 2004;31:185–197
56. Rossi DJ, Jamieson CH, Weissman IL. Stems cells and the pathways to aging and cancer. Cell. 2008;132:681–696
57. Lombard DB, Chua KF, Mostoslavsky R, et al. DNA repair, genome stability, and aging Cell. 2005;120:497–512
58. Rossi DJ, Bryder D, Seita J, et al. Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age. Nature. 2007;447:725–729
59. Rossi DJ, Seita J, Czechowicz A, et al. Hematopoietic stem cell quiescence attenuates DNA damage response and permits DNA damage accumulation during aging. Cell Cycle. 2007;6:2371–2376
60. Eaves FF III. Got evidence? Stem cells, bias, and the level of evidence ladder: Commentary on: “ASAPS/ASPS position statement on stem cells and fat grafting” Aesthet Surg J.. 2011;31:718–722
61. Eaves FF III, Rohrich RJ. So you want to be an evidence-based plastic surgeon? A lifelong journey. Aesthet Surg J.. 2011;31:137–142
62. Rohrich RJ, Eaves FF III. So you want to be an evidence-based plastic surgeon? A lifelong journey. Plast Reconstr Surg. 2011;127:467–472

©2014American Society of Plastic Surgeons


No comments

Be the first one to leave a comment.

Post a Comment