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Recent scientific advances in leiomyoma (uterine fibroids) research facilitates better understanding and management

[version 1; peer review: 5 approved]
PUBLISHED 06 Jul 2015
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Abstract

Uterine leiomyomas (fibroids) are the most prevalent medical problem of the female reproductive tract, but there are few non-surgical treatment options. Although many advances in the understanding of the molecular components of these tumors have occurred over the past five years, an effective pharmaceutical approach remains elusive. Further, there is currently no clinical method to distinguish a benign uterine leiomyoma from a malignant leiomyosarcoma prior to treatment, a pressing need given concerns about the use of the power morcellator for minimally invasive surgery. This paper reviews current studies regarding the molecular biology of uterine fibroids, discusses non-surgical approaches and suggests new cutting-edge therapeutic and diagnostic approaches.

Keywords

leiomyoma, uterine fibroids, uterine leiomyoma, fibroids, gynecological cancers

Introduction and context

The clinical management of uterine leiomyomas has advanced slowly and the current options remain limited. Advances in our understanding of the basic mechanisms of initiation and development over the past 5 years have elucidated the complexity of the molecular biology of leiomyomas. Although reviews of standard medical therapies have recently been published, this paper focuses on current findings in both basic and clinical research that have advanced the field and may open new strategies for treatment. Our goal is to open a dialog between clinicians and scientists to stimulate additional treatment options for women with uterine leiomyomas.

Background

Leiomyomas, also called fibroids due to their abundant fibrotic tissue, have a 70–80% cumulative incidence in the childbearing years1. These benign tumors are known to clinicians as a worldwide public health problem. Estimates of treatment costs of leiomyomas in the US range from $5.9 billion to $34.4 billion annually, and includes the costs of medical and surgical treatment, amount of work time lost and complications attributable to the tumors2. These data suggest the estimated costs contribute more to health care expenditures than breast, colon or ovarian cancer2. The symptoms of uterine leiomyomas include bleeding with possible subsequent severe anemia, symptoms of pain and pressure leading to difficulty with bowel and bladder function and, in some cases, infertility and pregnancy complications. Notably, the tumors may arise anywhere in the uterine myometrium necessitating individualization of therapy. Large tumors may present with few if any symptoms while small fibroids may cause severe bleeding and pain. Hysterectomy is a common treatment that unfortunately negates the possibility of childbearing. Hysterectomy aside, subserosal or intramural fibroids can negatively impact fertility3. Currently, the decisive treatment is hysterectomy, either via abdominal/vaginal route or increasingly through laparoscopic incisions. Myomectomy, the surgical removal of only tumors, is a popular therapeutic option because it preserves childbearing, an important consideration for women of reproductive age. Uterine artery embolization, and MRI guided focused ultrasound and radiofrequency ablation are also suitable for some women.

Many advances have occurred over the past 5 years and are reviewed here briefly as they have changed our understanding of the nature of leiomyoma. Without this critical basic understanding, advances in non-invasive therapies cannot be developed and optimal individualized therapies adopted.

Advances in basic studies

African-Americans develop benign leiomyomas at younger ages than Caucasians. The tumors appear to decrease in their growth rates before menopause in Caucasians but no decrease in growth is apparent in African-Americans4. Although this finding was published in 2008, it has not always been appreciated by active clinicians and researchers. Reported similarities between leiomyomas and keloids5,6 are consistent with recent findings7. Leiomyoma cells secrete high levels of disarrayed and altered collagen fibrils, fibronectin, and other extracellular matrix components and resist apoptosis6,8,9. Fibroids vary in uterine location and size up to 20 cm, or greater. One individual may have only one tumor while another might have multiple tumors. Growth is influenced by female gonadal steroids. However, the steroid-dependent growth is tumor-specific and not systemic as the same individual uterus may present multiple fibroids having differing growth patterns—some grow, some regress, and some are stable in the same time period4. Thus, leiomyomas exhibit complex mechanisms of development and growth.

Mechanotransduction, the response of cells to the mechanical forces such as compression and stretch, influences the biochemical pathways in all cells that affect growth at the cellular and tissue level1012, including wound healing responses5, growth factors, reproductive hormones and cytokines13, and uterine stem cells14,15. Three recent reviews on the topic of mechanotransduction in reproduction expand in detail on this signaling mechanism1012. Increasing evidence suggests a role for mechanotransduction in leiomyoma initiation and growth. Both biomechanical and biochemical factors, and not merely one paramount molecule, cause changes in uterine smooth muscle and leiomyoma cell behavior10. These changes occur through bi-directional signaling from individual cells to their matrix microenvironment and back to fibroid cells10. Catastrophic genetic alterations called chromothripsis, a sudden episode of chromosomal shattering and rearrangement, have been found in uterine fibroids16. However, not all leiomyomas display these genetic alterations; thus it is not clear whether the genetic defects are a primary cause or only associated with the development of some tumors. A recent study analyzed the genetic abnormalities in 256 fibroid tumors from 120 women17. In this study, 20 (7.8%) of the fibroids had a chromosomal rearrangement of 12q14-15 reflecting the rearrangement of the HMGA2 allele, while 179 (69.9%) of the fibroids exhibited a mutation of mediator complex subunit 12 (MED12), a transcription factor gene17. The remaining 22.3% of the tumors were reported as having either another genetic abnormality or no detectable abnormality17. Similar findings were recently found in a population of 135 women from the Southern United States with 64.33% of the fibroid tissues having MED12 mutations in exon 2 including deletion mutations18. Uterine smooth muscle cells respond to mechanotransduction in a different manner from cardiac muscle, which suggests that their innate qualities are unique19. One interesting aspect of leiomyomas is that they are surrounded by a relatively thick wall, a pseudocapsule, which encapsulates the tumors. Investigations of mutations in the MED12 gene have demonstrated that the pseudocapsule is derived from surrounding myometrium and not the tumor itself20. Understanding of pseudocapsule development may reveal new therapeutic targets.

Interestingly, while fibroids are clonal tumors, each arising from a single cell, they are grossly and molecularly heterogeneous growths, consisting of the considerable extracellular matrix that provides the characteristic property of tumor stiffness noted on clinical palpation21. Leiomyomas are rare in animals and there is no universally-accepted spontaneous animal model. The Eker rat develops tumors that resemble fibroids, but the growths do not exhibit the abundant collagen characteristic of the human tissue22. While murine models have been reported, they have not been widely adopted.

Currently, research in the field relies on human tissues and cultured cells from surgical specimens, but the tumor or tumor-derived cells being studied might be in a state of active growth, or alternatively senescence at the time of acquisition. This fact is a significant consideration for the field. Because of this complexity, the identification of key molecular pathways in tumor development remains elusive and presents challenges to pharmaceutical development.

Recent advances in clinical treatment

Clinical management decisions revolve around control of the heavy menstrual bleeding, including anemia which is often severe, chronic pain and pressure, or infertility. These symptoms are severe enough in approximately 25% of women with fibroids to require treatment13. Here we review pertinent advances and suggest areas of further avenues of inquiry. Several recent articles review in detail the treatment options currently available, including herbal medications2326, and provide clinicians with comprehensive up-to-date information for treatment decision-making. Strategies for prevention or reduction in fibroid growth rate in high-risk women may be possible, as reviewed in Table 12736. It is worth mentioning that, in addition, multiple in vivo and animal studies suggest that Vitamin D presents an attractive strategy to prevent uterine fibroid formation3742, and hopefully clinical trials will show the efficacy of this approach.

Table 1. Strategies for prevention and reduction of growth rate of uterine fibroids.

StudyStudy
design
nTreatment
period
Treatment
regimen/dose
Main study
results
Statistical
significance
Summary of effects
Green tea extract
(epigallocatechin gallate:EGCG)
Zhang et al. 201027 In vivo
Xenograft
Tumors in
mice
n.a.8 weeksPlacebo
(H2O)
TFV
288±57
P<0.05EGCG significantly
reduced TFV vs.
placebo in nude
mouse model
EGCG 1.25mg/d129±54
Roshdy et al. 201328 334 monthsPlacebo% TFV
+24.3
P≤0.05EGCG significantly
reduced TFV, while
TFV increased with
placebo. Reduced
symptom severity,
improved QOL and
anemia
EGCG 800mg/d% TFV
-32.6
P<0.0001
Curcumin
Malik et al. 200929 In vitro n.a.48 hoursNo curcumin,
Curcumin
5–40μM
Fibroid cell
growth:
All decreased
P<0.05Curcumin
decreased fibroid
cell proliferation at
all concentrations.
20μM curcumin
inhibits fibroid
cells, insignificant
impact on matched
myometrial cells
P<0.05
Tsuiji et al. 201130 In vitro n.a.3 daysDMSO (0.1%)
Curcumin
100–500μM
Curcumin
>200μM inhibits
fibroid cell growth
P<0.01Curcumin over 200μM
significantly inhibited
cell growth compared
to control via PPARγ
activation in fibroid cells
Depot-
medroxprogesterone
acetate (DMPA)
Lumbiganon et al.
199631
CC910n.a.Controls
(n=2709)
DMPA use 25.6%OR [95% CI]
0.44 (0.36–0.55)
DMPA significantly
protective against UF
volume: persists >10
yrs after last dose
Cases (n=910)DMPA use 13.3%
Venkatachalam et al.
200432
Cohort206 monthsDMPA
150mg/month
TFV
-33%
P<0.001DMPA significantly
reduces UF volume in
6 months
Progestin releasing
intrauterine system
(Levonorgestrel-
releasing
intrauterine system:
LNG-IUS)
Sayed et al. 201133 RCT5912 monthsLNG-IUS
vs.COC
PBAC score (%)
LNG-IUS=88±16.5
COC=53.5±51.2
p=0.02LNG-IUS more
effective than COC in
reducing menstrual
bleeding.

Change in fibroid
diameter did not
occur.
Fibroid Diameter
adjusted to
uterine volume
(From Table 3)
LNG- IUS=Baseline
2.4±1.4
Treated 2.5±1.5
COC=Baseline
2.7±1.4
Treated 2.8±1.3
p=0.53 after
treatment
Combined Oral
Contraceptive Pills
(COC)
Qin et al. 201334 MA11 cohort
and CC
studies
n.a.COC useRR
[95% CI]
n.a.Meta-analysis
indicates current
use of COC does
not increase fibroid
morbidity
Study heterogeneity
present
Conclusion: COCs do
not increase risk for
fibroids and thus COC
should be prescribed
when indicated
Ever use
(1–5 yrs)
0.88 (0.73-1.07)
Ever use (>5
yrs)
0.83 (0.69–0.99)
Current use0.43 (0.25–0.73)
Former use0.96 (0.84–1.08)
25-(OH) Vitamin D
Sabry et al. 201335 CC154n.a.Measured
serum 25-(OH)
vitamin D
correlated with
fibroid number
and volume as
determined by
TVUS
Lower serum
25-(OH) vitamin D
levels associated
with occurrence
of fibroids
correlates with
volume
P=0.01
r=0.31
P=0.002
Lower serum vitamin
D correlates inversely
with total uterine
volume in black
subjects, but not
significant in whites.
Halder et al. 201436 In vivo
Xenograft
nude
mouse
model
and
uterine
fibroid
cells
n.a.Paracalcitrol
300ng/kg/day
or
1, 25
di-hydroxy
vitamin D
500ng/kg/
day

Vehicle
controls
4 weeks∙ P-calcitrol
Reduced cell
growth 9%
∙ vitamin D
reduced cell
growth 1%
∙ Reduced fibroid
size
∙ Collagen
reduced in
culture
P<0.05Reduced tumor size,
but paracalcitrol was
more effective.

Abbreviations: CC, case control; COC, combined oral contraceptive pill; DMSO, dimethyl sulfoxide; DMPA, depot medroxyprogesterone acetate; EGCG, epigallocatechin gallate; LNG-IUS, levonorgestrel-releasing intrauterine system; OR, odds ratio; PBAC, Pictorial Pain, Bleeding Assessment Chart; PPARγ, peroxisome proliferator-activated receptor gamma; QOL, quality of life; RR, relative risk; TFV, Total fibroid volume; TVUS, transvaginal ultrasound; UF, uterine fibroid.

Currently, there is no simple, effective screening method to determine if a uterine tumor is indeed benign and not malignant, prior to treatment. It is known that adenomyosis can present clinically in a manner suggestive of fibroids. Recently, it was reported that experienced physicians using preoperative ultrasonograms interpreted myometrial hyperplasia on tissue histopathology as uterine fibroids43. This study suggests that preoperative ultrasound imaging using current standard technology may be responsible for over diagnosing uterine fibroids. However, the misdiagnosis of leiomyosarcoma is of greater concern. A strategy to determine if a tumor is a leiomyosarcoma is urgently needed. MRI techniques demonstrate the ability to differentiate malignant from benign tumors44 but have not yet been validated indistinguishing leiomyosarcoma from leiomyoma. While important, this approach is clearly not cost-effective. Using shear wave elastography, a leiomyosarcoma was accurately diagnosed pre-operatively, based on the degree of stiffness throughout the tumor45. If this modality were confirmed in larger studies, it would be a major breakthrough for the field. Specifically, power morcellation has been restricted as a modality, even though it reduces complications4648, but a reliable pre-treatment tool to diagnose leiomyosarcoma would renew interest in that method.

Ulipristal acetate was developed as a selective progesterone receptor modulator with pure progesterone receptor antagonistic activity and minimal antiglucocorticoid effects. Ulipristal is currently marketed as Esmya and was approved by the FDA in 2010 for emergency contraception. It is approved in Europe and Canada for pre-surgical treatment of fibroids. One or three month courses of ulipristal acetate has been shown to induce apoptosis and to decrease proliferation of uterine fibroid cells, and to decrease fibroid size by a variable amount. No relevant affinity for estrogen, androgen or progesterone receptors (ER, AR or PR) has been observed. Several randomized trials demonstrated that ulipristal decreased the volume of leiomyomas significantly in comparison to controls4951. Ulipristal has also been shown to induce amenorrhea4951. Ulipristal does not induce changes in gonadotropin releasing hormone (GnRH) levels and does not reduce serum estradiol levels below the 50 pg/dl levels necessary to maintain bone mineral density52,53. For many women the advantage of this non-surgical treatment is the ability to preserve fertility. The first study of pregnancy after completed ulipristal treatment was recently published53. Of 21 women who had stopped ulipristal and attempted pregnancy, a pregnancy occurred in 15 women (71%) with 18 pregnancies during the study period with no regrowth of the leiomyomas. Twelve pregnancies produced healthy live infants and 6 resulted in spontaneous abortion (miscarriage)53. Other selective progesterone modulators, such as proellex, are currently being evaluated and Elagolix, an orally administered formulation of GnRH, is currently being studied in clinical trials.

Possible new therapies on the horizon

A purified bacterial collagenase from Clostridium histolyticum (CCH) has recently been shown in ex vivo leiomyoma tissue to significantly degrade the altered collagen when injected into tumor tissue. When the concentration of the CCH was increased and the injection volume kept small, the penetration of the CCH into the myometrium was limited and indicates that, on refinement of the dose, penetration into the myometrium could be eliminated. CCH is inhibited by serum proteins, a fact which also mitigates the concern for damage to the myometrium. Most importantly, our group in collaboration with Farshid Guilak and his colleagues at Duke University have shown that this collagenase (already FDA approved for use in the treatment of hand contractures due to collagen cord formation and for a disease of the male penis due to abnormal collagen formation), clearly reduced tissue stiffness in leiomyomas54. This reduced stiffness would not only reduce the bulk of the tumor, it is theoretically capable of altering mechanical signaling pathways in the leiomyoma, overcoming the resistance to apoptosis and allowing the cells to die. Clinical studies have demonstrated that the collagenase does not affect blood vessels or nerves. The use of CCH, alone or with other drugs such as a selective progesterone receptor modulator, could potentially be utilized as an injectable therapy for uterine leiomyomas 3–7 cm in size and could be most useful in treating submucosal leiomyomas, the type most associated with infertility55.

The development of materials designed to deliver and protect drug therapeutics by direct injection to the tumor site is an area of active research. Several such drug delivery materials that change phase in response to temperature changes are currently in development as they offer many advantages over conventional drug delivery systems23. These thermoresponsive materials form a solution in aqueous media that reversibly transitions to a gel at physiological temperatures. The system often degrades in a defined period of time, thereby eliminating the need for surgical explantation. In its solution state, the delivery system readily mixes with therapeutic agents to afford a drug formulation that can be administered by a single injection. The injected formulation is a stable solution that transforms into a gel depot at the site of injection as a result of an elevation in temperature.

The marriage of injectable thermoresponsive delivery systems with the unmet need for viable non-surgical options for the management of uterine fibroids offers several advantages. Creating a drug depot inside the fibroid by local injection would impede diffusion and distribution of the drug away from the injected fibroid, prolong release, delay inactivation, and therefore reduce the need for repeat injections. This treatment approach for women wanting to maintain fertility yet seeking relief from fibroid symptoms could be administered by skilled individuals under ultrasound guidance in a doctor’s office. A few examples of the most promising of these thermoresponsive delivery systems are given below (Table 2).

Table 2. Thermoresponsive biodegradable injectable drug delivery systems.

AtriGel®ReGel™LiquoGel™
DescriptionPolymer (1 unit) for physically delivering
entrapped pharmaceuticals
Copolymer (3 units) for physically
delivering entrapped pharmaceuticals
Copolymer (4 units) for physically
delivering entrapped and/or
covalently linked pharmaceuticals
PropertiesWater-insoluble
Biodegradable
Liquid: < 0°C – 30°C
Gel: 37°C
Water soluble
Biodegradable
Liquid: < 0°C – 30°C
Gel: 37°C
Water soluble
Biodegradable
Liquid: <4°C – 30°C
Gel: 37°C
Mechanism of
Drug Release
Diffusion and polymer erosionDiffusion and polymer erosionDiffusion and polymer erosion
Drug Release
Delay
4–6 weeks6–8 weeks12–15 hours
CompositionPolymer platform consisting of one of the
following:
PLA1, PLG2, PLC3, PAH4
Triblock copolymer of:
PLGA-PEG-PLGA
4 Components:
Acrylic Acid
Polyglycerol
N-Isopropylaniline
HEMA-Lac5
HPG-MA6
Recent
applications
Testosterone reduced: Clinical studies using
a depot containing 22.5 mg leuprolide
maintained an effective suppression
of serum testosterone (50 ng/dL) for more than
3 months.
Cancer: Single drugs were
incorporated including paclitaxel,
porcine growth hormone,
glucagon-like peptide-1 (GLP-1),
interleukin 2 (IL-2) and G-CSF
Uterine Fibroids: In Development

Notes: 1poly(DL-lactide); 2poly(DL-lactide-do-glycolide); 3poly(DL-lactide-co-caprolactone); 4polyanydrides; 5hydroxyethyl methacrylate-polylactide; 6Hyperbranched polyglycerol. Modified from reference 23

One material developed by our group and listed in Table 2 is particularly worth noting. LiquoGel™ delivers drugs similar to other thermoresponsive delivery systems but distinguishes itself from other materials in that it contains multiple functional groups that enable chemical modifications to covalently link therapeutics. Thus, multiple drugs can be delivered at one time. With the advent of the means to deliver drugs or drug combinations directly to leiomyoma tumors, the potential of reduction and perhaps eradication of tumors prior to the need for surgical or other major interventions (such as focused ultrasounds or uterine artery embolization) could be realized. Multiple drugs could be given as combination chemotherapy, such as an anti-fibrotic agent combined with a selective progesterone receptor modulator, or sequentially, for the benefit of patient care. It could be possible to deliver gene therapy in this manner as well5558. A number of the more conventional drug therapies for uterine fibroids could be potentially entrapped or covalently linked to LiquoGel™ to afford delivery with potentially reduced side effects, improved efficacy, and controlled release profiles23.

Implications for clinical practice

Even though treatments for fibroids can be developed currently without a complete elucidation of their etiology and molecular biology, ultimately, if the molecular mechanisms for fibroid development and of myometrial proliferation are understood, additional nonsurgical therapeutic interventions may be forthcoming. Taken together, we have evidence that uterine leiomyomas grow due to cell proliferation, but even more because of excessive deposition of altered extracellular matrix due to the persistence of secreting cells. There is a growing appreciation of the complex pathways leading to the formation of uterine leiomyomas which will lead to new therapeutic approaches. Could drug therapy, either a single drug or most likely combination chemotherapy, rival the effectiveness of surgical procedures yet preserve the uterine childbearing function? If realized, could such a therapy be administered during a routine visit to the doctor or clinic? Addressing these questions presents unique opportunities at the interface of molecular medicine and clinical care.

The optimal treatment remains one that reduces the bulk of the leiomyoma and reduces blood loss while preserving the ability to have children. Clinician, doctors, patients, and researchers should continue to work together to develop cost-effective and efficacious solutions to leiomyoma disease that are compatible with the woman’s life-style, reducing or eliminating hospital stay and lengthy recovery time23.

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Taylor DK, Holthouser K, Segars JH and Leppert PC. Recent scientific advances in leiomyoma (uterine fibroids) research facilitates better understanding and management [version 1; peer review: 5 approved]. F1000Research 2015, 4(F1000 Faculty Rev):183 (https://doi.org/10.12688/f1000research.6189.1)
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Reviewer Report 14 Jul 2015
Pasquapina Ciarmela, Polytechnic University of Marche, Ancona, Italy 
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Ciarmela P. Reviewer Report For: Recent scientific advances in leiomyoma (uterine fibroids) research facilitates better understanding and management [version 1; peer review: 5 approved]. F1000Research 2015, 4(F1000 Faculty Rev):183 (https://doi.org/10.5256/f1000research.6634.r9486)
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Reviewer Report 06 Jul 2015
Andrea Tinelli, Department of Gynecology and Obstetrics, Vito Fazzi Hospital, Lecce, Italy 
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Tinelli A. Reviewer Report For: Recent scientific advances in leiomyoma (uterine fibroids) research facilitates better understanding and management [version 1; peer review: 5 approved]. F1000Research 2015, 4(F1000 Faculty Rev):183 (https://doi.org/10.5256/f1000research.6634.r9356)
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Reviewer Report 06 Jul 2015
Alicia Armstrong, Contraceptive Discovery and Development Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD, USA 
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Armstrong A. Reviewer Report For: Recent scientific advances in leiomyoma (uterine fibroids) research facilitates better understanding and management [version 1; peer review: 5 approved]. F1000Research 2015, 4(F1000 Faculty Rev):183 (https://doi.org/10.5256/f1000research.6634.r9355)
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Reviewer Report 06 Jul 2015
Ayman Al-Hendy, Department of Obstetrics and Gynecology, Georgia Regents University, Augusta, GA, 30912, USA 
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Al-Hendy A. Reviewer Report For: Recent scientific advances in leiomyoma (uterine fibroids) research facilitates better understanding and management [version 1; peer review: 5 approved]. F1000Research 2015, 4(F1000 Faculty Rev):183 (https://doi.org/10.5256/f1000research.6634.r9354)
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Donna Day Baird, Laboratory of Women’s Health, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA 
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Baird DD. Reviewer Report For: Recent scientific advances in leiomyoma (uterine fibroids) research facilitates better understanding and management [version 1; peer review: 5 approved]. F1000Research 2015, 4(F1000 Faculty Rev):183 (https://doi.org/10.5256/f1000research.6634.r9353)
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