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1 LNCaP bone tumors were both osteoblastic and osteolytic.
2 derately osteoblastic LM8 (P < 0.05) and the osteolytic 143B (P < 0.01) cell line-derived tumors.
3 that give rise to advanced bone cancer pain, osteolytic 2472 sarcoma cells or media were injected int
4  pain, we used an in vivo model where murine osteolytic 2472 sarcoma cells were injected and confined
5                          The majority of the osteolytic (72; 93.5%) and mixed-pattern lesions (nine;
6           The 146 lesions were classified as osteolytic (77), osteoblastic (41), mixed-pattern (11),
7 NKL) with osteoprotegerin (OPG) prevents the osteolytic activity of CaP and its ability to establish
8  expression of target genes that mediate the osteolytic activity of metastatic breast cancer cells.
9 eoblastic activity, but had no effect on its osteolytic activity.
10 aled the mixed bone lesions, comprising both osteolytic and osteoblastic elements.
11 ese effects were enhanced in the presence of osteolytic and osteoblastic factors such as RANKL (recep
12 s can be useful tools in characterizing pure osteolytic and osteoblastic lesions induced by human pro
13 andardized uptake values [SUVs]) of 18FDG in osteolytic and osteoblastic metastases were compared.
14 pressing LNCaP cells (LNCaP-PDGF-D) revealed osteolytic and osteoblastic responses similar to those o
15 tably, the model revealed distinct phases of osteolytic and osteogenic activity, a critical role for
16                     We review the biology of osteolytic and osteosclerotic lesions, with a focus on e
17 ce for close interplay between inflammatory, osteolytic and tumor cell-driven events in the bone-tumo
18 inally assess the formation of osteoblastic, osteolytic, and mixed lesions formed by human prostate c
19 ppears to be the centerpiece of inflammatory-osteolytic arthritis and direct inhibition of this trans
20   Interestingly, ATL cells overexpressed the osteolytic-associated genes-Wnt5a, PTHLH, and RANKL.
21 teum, similar to that found in patients with osteolytic bone cancer.
22                                              Osteolytic bone destruction and its complications, bone
23                                          The osteolytic bone destruction associated with breast cance
24  a tumor-bone co-culture system and enhances osteolytic bone destruction in mice, but also inhibits o
25 a support a model in which tumor cells cause osteolytic bone destruction independently of the RANK li
26 d with human metastatic bone disease such as osteolytic bone destruction.
27 al for the development of metastasis-related osteolytic bone destruction.
28 ould decrease PTHrP expression and therefore osteolytic bone destruction.
29 a key role in the pathogenesis of MM-related osteolytic bone disease (OBD).
30 factor, osteoprotegerin, were protected from osteolytic bone disease and developed fewer soft-tissue
31 masome-independent production of IL-1beta in osteolytic bone disease and identify PSTPIP2 as a negati
32 roid hormone-related peptide (PTHrP), namely osteolytic bone disease associated with breast cancer an
33 y multiple myeloma (MM) cells contributes to osteolytic bone disease by inhibiting the differentiatio
34 y play a critical role in the development of osteolytic bone disease in multiple myeloma and that tar
35  Il1r and Il1beta, but not Il1alpha, rescued osteolytic bone disease in mutant mice.
36 ized the osteoimmunological underpinnings of osteolytic bone disease in Pstpip2(cmo) mice.
37                                              Osteolytic bone disease is a major cause of morbidity in
38 del, treatment with NB-DNJ markedly improved osteolytic bone disease symptoms.
39 e marrow, elevated serum immunoglobulin, and osteolytic bone disease.
40 onment in myeloma counteracts development of osteolytic bone disease.
41  multiple myeloma progression and associated osteolytic bone disease.
42 ls in the bone marrow and the development of osteolytic bone disease.
43 ted with tumor growth within bone marrow and osteolytic bone disease.
44  can promote myeloma growth and survival and osteolytic bone disease.
45 oma (MM), particularly in the development of osteolytic bone disease.
46 nists for the treatment of MM and associated osteolytic bone disease.
47 on of GSLs in osteoclast (OC) activation and osteolytic bone diseases in malignancies such as the pla
48 identify increased numbers of osteoclasts in osteolytic bone diseases such as osteolytic bone metasta
49 new therapeutic approaches to combat various osteolytic bone diseases.
50 ie2 activity in vivo significantly inhibited osteolytic bone invasion and tumor growth in a mammary t
51 w function of Tie2 in osteoclastogenesis and osteolytic bone invasion of breast cancer.
52                                 The risk for osteolytic bone lesion complications in metastatic breas
53 f symptomatic MM is a well-demarcated, focal osteolytic bone lesion.
54    Multiple myeloma (MM) is characterized by osteolytic bone lesions (OBL) that arise as a consequenc
55 splacement of hematopoiesis and formation of osteolytic bone lesions also known as myeloma bone disea
56 major contributing factor to the increase in osteolytic bone lesions and hypercalcemia found in ATL p
57 read dissemination of tumor cells leading to osteolytic bone lesions and liver metastases, common sit
58 t increased IL-1 signaling can cause aseptic osteolytic bone lesions and that the absence of IL-10 si
59  acid phosphatase to confirm the presence of osteolytic bone lesions and the presence of osteoclasts,
60 andibular alveolar processes for presence of osteolytic bone lesions around causative teeth roots and
61 nt pathogenetic role in the establishment of osteolytic bone lesions in breast cancer.
62 day) significantly reduced the occurrence of osteolytic bone lesions in myeloma-bearing mice.
63 sk of skeletal complications associated with osteolytic bone lesions in patients with breast cancer a
64 r an effective therapeutic approach to treat osteolytic bone lesions in patients with myeloma.
65                 Strong TGF-beta signaling in osteolytic bone lesions is suppressed directly by geneti
66 timyeloma therapy, regardless of presence of osteolytic bone lesions on conventional radiography.
67    Multiple myeloma (MM) is characterized by osteolytic bone lesions with uncoupled bone remodeling.
68 prevented myeloma-induced bone loss, reduced osteolytic bone lesions, and increased fracture resistan
69 cells may be important in the hypercalcemia, osteolytic bone lesions, neutrophilia, elevation of C-re
70                                Specifically, osteolytic bone lesions, where bone is destroyed, lead t
71    Breast cancer (BCa) bone metastases cause osteolytic bone lesions, which result from the interacti
72 oclast formation, and radiologic evidence of osteolytic bone lesions.
73 E suppressed bone colonization and decreased osteolytic bone lesions.
74 t was expressed in two of three specimens of osteolytic bone metastases (P=0.0119).
75 develop radiographically detectable multiple osteolytic bone metastases and cachexia in this model.
76 e that Smad4 contributes to the formation of osteolytic bone metastases and is essential for the indu
77 u-RGD has the potential to effectively image osteolytic bone metastases and monitor the physiologic c
78 (RGDyK) ((64)Cu-RGD) as an imaging agent for osteolytic bone metastases and their associated inflamma
79 ed, inhibited the progression of established osteolytic bone metastases as assessed by radiographic a
80 mor inoculation prevented the development of osteolytic bone metastases compared with vehicle.
81 cer cells may be vital to the development of osteolytic bone metastases in patients with breast cance
82 s to bone, we used an in vivo model in which osteolytic bone metastases preferentially occur after in
83 usly developed hypercalcemia, high-frequency osteolytic bone metastases, and enhanced osteoclast acti
84 y promoting hypercalcemia, tumor growth, and osteolytic bone metastases, but it is not known how PTHr
85 east cancer cells, which consistently formed osteolytic bone metastases, induced osteosclerotic lesio
86 eature of our findings was the occurrence of osteolytic bone metastases, which are prominent in human
87 d that seven different mouse models of human osteolytic bone metastases-representing breast, lung and
88 THrP-neutralizing antibody greatly decreased osteolytic bone metastases.
89 tases, induced osteosclerotic lesions in the osteolytic bone metastases.
90  the use of bisphosphonates in patients with osteolytic bone metastases.
91  the use of bisphosphonates in patients with osteolytic bone metastases.
92 n women with stage IV breast cancer who have osteolytic bone metastases.
93 eoclasts in osteolytic bone diseases such as osteolytic bone metastasis and inflammatory osteolysis.
94  animal model of high-penetrance spontaneous osteolytic bone metastasis and underscore the critical r
95         EGF receptor (EGFR) inhibitors block osteolytic bone metastasis by targeting EGFR signaling i
96  into the left cardiac ventricle resulted in osteolytic bone metastasis in 74% of beta3+/+ mice by 14
97 rolling not only tumor angiogenesis but also osteolytic bone metastasis in breast cancer.
98 ious carcinomas such as breast cancer, where osteolytic bone metastasis is associated with increased
99                     We further observed that osteolytic bone metastasis led to a decrease in HA nanoc
100 rget of NF-kappaB and found that it mediates osteolytic bone metastasis of breast cancer by stimulati
101 ppaB (NF-kappaB) plays a crucial role in the osteolytic bone metastasis of breast cancer by stimulati
102 to evaluate the mechanism of MMP13-dependent osteolytic bone metastasis revealed that MMP13-ASO treat
103 over a new and specific role of NF-kappaB in osteolytic bone metastasis through GM-CSF induction, sug
104 e inoculated with MDA-MB-231 cells developed osteolytic bone metastasis without hypercalcemia or incr
105 id hormone-related protein (PTHrP), enhanced osteolytic bone metastasis, and decreased survival.
106 al for the bone resorption characteristic of osteolytic bone metastasis.
107 ting tumor-stromal interactions that promote osteolytic bone metastasis.
108 ncer and implicate Rho-TGF-beta crosstalk in osteolytic bone metastasis.
109 ivo inhibits osteoclast activity and reduces osteolytic bone metastasis.
110 wed that they have the ability to reduce the osteolytic bone resorption associated with multiple myel
111 g DKK1 activity in myelomatous bones reduces osteolytic bone resorption, increases bone formation, an
112 Wu et al. identify MAOA as a key mediator of osteolytic bone responses that involve complex paracrine
113 or cells regulates processes associated with osteolytic bone tumor burden, we stably infected the bon
114  a unique expression signature that promotes osteolytic breast cancer bone metastasis and that inhibi
115 ior to bone scintigraphy in the detection of osteolytic breast cancer metastases, which led to a poor
116  in immune-compromised animals bearing human osteolytic cancers.
117              Using a mouse model that mimics osteolytic changes associated with breast cancer-induced
118                                  CT revealed osteolytic changes in 41 (31%) and osteoblastic changes
119 PTHLH), leading to osteoclast maturation for osteolytic colonization.
120 ls perpetuate the inflammatory response, the osteolytic component of this disease is a direct result
121  may block TGF-beta propagation of a vicious osteolytic cycle in this MDA-MB-231 model of bone metast
122 sequently, pDC and CD4(+) T cells, producing osteolytic cytokines, increased with tumor burden, causi
123 duce a profound decrease in tumor burden and osteolytic damage in the murine 5TGM1 model of MM bone d
124 1beta expression precedes the development of osteolytic damage in young Pstpip2(cmo) mice, and geneti
125      Conventional radiographs showed a small osteolytic defect in the anterior cortex of the midtibia
126 round also demonstrated striking spontaneous osteolytic destruction of distal phalanges.
127          Survival was lower in patients with osteolytic disease compared with the remainder (P=.01).
128  myeloma cells also reduced the formation of osteolytic disease in vivo after intratibial engraftment
129  mechanism by which Runx2 contributes to the osteolytic disease induced by MDA-MB-231 cells, we inves
130 ion of factors involved in the generation of osteolytic disease remain elusive.
131 ivin A levels were found in MM patients with osteolytic disease.
132 one-resorbing factors (PTHrP, IL8) promoting osteolytic disease.
133 2 short hairpin RNA inhibition prevented the osteolytic disease.
134 s and the bone microenvironment that lead to osteolytic disease.
135                                              Osteolytic diseases, including rheumatoid arthritis, ost
136 heumatoid arthritis, osteoporosis, and other osteolytic disorders.
137 rP, consistent with its previously described osteolytic effects in metastatic bone disease, can also
138                     To determine whether the osteolytic factor parathyroid hormone-related protein (P
139 ich in turn increases secretion of important osteolytic factors such as parathyroid hormone-related p
140 one-invasive oral SCC (OSCC) derived from an osteolytic feline OSCC.
141                  C3H mice were injected with osteolytic fibrosarcoma cells in and around the calcaneu
142                      Unilateral injection of osteolytic fibrosarcoma cells into and around the calcan
143        When tumors formed after injection of osteolytic fibrosarcoma cells into the calcaneus bone of
144 se-directed processing of PTHrP disables the osteolytic functions of the mature hormone to promote os
145 x polymicrobial biofilm-induced inflammatory osteolytic gingival infection that results in orofacial
146 his study, we report that DKK-1 knockdown in osteolytic human PCa cells unexpectedly delays the devel
147 anism for modulating osteoclast signaling in osteolytic inflammatory disease.
148      Therapies to reverse tissue damage from osteolytic inflammatory diseases are limited by the inab
149 eering approach for the treatment of chronic osteolytic inflammatory diseases.
150                  In a PC-3M-luc cell-induced osteolytic intraosseous model of prostate cancer, these
151 ue involvement, presence of an abscess or an osteolytic lesion around causative tooth.
152  mechanisms of inhibiting myeloma growth and osteolytic lesion development.
153 r interactions governing the early events of osteolytic lesion formation are currently unclear.
154                                Surprisingly, osteolytic lesion formation was greatest in animals lack
155 tumours or systemic delivery of LOX leads to osteolytic lesion formation whereas silencing or inhibit
156 issemination in the bone marrow and enhanced osteolytic lesion formation, irrespective of HIF-1 Conve
157 er cells in the bone marrow and tumor-driven osteolytic lesion formation.
158  the progression of soft tissue necrosis and osteolytic lesion formation.
159 tion of LOX activity abrogates tumour-driven osteolytic lesion formation.
160     Infection of the dental pulp leads to an osteolytic lesion that results from a polymicrobial infe
161 ved to be central to the pathogenesis of the osteolytic lesion, the mechanisms by which this bacteria
162 ctures (45 [5%] vs 66 [7%]; p=0.04), and new osteolytic lesions (46 [5%] vs 95 [10%]; p<0.0001).
163                          After treatment, 58 osteolytic lesions (80.5%) became [(18)F]FDG negative an
164 es that produce osteoblastic (MDA PCa 2b) or osteolytic lesions (PC-3).
165    CCR1 activation leads to the formation of osteolytic lesions and facilitates tumor growth.
166 toma cells recruited osteoclasts to generate osteolytic lesions and invade the bone matrix.
167 use model of bone metastasis, A77636 reduced osteolytic lesions and prevented mechanical weakening of
168  progeria-like disease phenotypes, including osteolytic lesions and rib fractures, osteoporosis, slow
169                                              Osteolytic lesions are a painful consequence of metastas
170 s that these compounds reduce PTHrP-mediated osteolytic lesions associated with metastatic human brea
171 , our findings suggest a novel mechanism for osteolytic lesions caused by cancer cells metastasizing
172  treatment completely prevented radiographic osteolytic lesions caused by human MDA-MB-231 breast can
173 l analysis at weekly intervals revealed that osteolytic lesions developed in the control tibias by 2
174     Anti-Wnt5a therapy may prevent or reduce osteolytic lesions found in ATL patients and improve the
175           Multiple myeloma is incurable once osteolytic lesions have seeded at skeletal sites, but fa
176 s may correlate with a propensity to develop osteolytic lesions in arthritis.
177 pose tissue, micrognathia, osteoporosis, and osteolytic lesions in bone.
178 reast cancer cells can prevent production of osteolytic lesions in bone.
179 lopecia, micrognathia, dental abnormalities, osteolytic lesions in bones, and osteoporosis, which are
180 at MMP-13 is critical for the development of osteolytic lesions in MM and that targeting the MMP-13 p
181 activity of osteoblasts (OBs) contributes to osteolytic lesions in multiple myeloma (MM).
182  very effective in limiting the formation of osteolytic lesions in PC-3 implanted tibias by inhibitin
183                                              Osteolytic lesions in the ribs led to spontaneous bone f
184 on of DKK1 by MM cells likely contributes to osteolytic lesions in this disease by inhibiting Wnt sig
185 n several human cancer cell lines that cause osteolytic lesions in vivo and produce PTHrP (MDA-MB-231
186 ort that human neuroblastoma cells that form osteolytic lesions in vivo do not produce osteoclast-act
187  tumor cells abolishes their ability to form osteolytic lesions in vivo.
188 n osteoblastic reaction in vitro and induced osteolytic lesions in vivo.
189  bone scans have sensitivity limitations for osteolytic lesions manifested in MM.
190 veloped hypercalcemia and significantly more osteolytic lesions than mice bearing CHO/EV tumors, with
191 a cells in the bone marrow induces localized osteolytic lesions that rarely heal due to increased bon
192                                Total area of osteolytic lesions was significantly lower in mice treat
193 ith established bone metastases, the size of osteolytic lesions was significantly reduced after 4 wee
194 bone marrow plasma from femurs affected with osteolytic lesions were increased 2.5-fold over correspo
195                                  Microscopic osteolytic lesions were observed adjacent to plasma cell
196  osteolysis in mice receiving control cells, osteolytic lesions were significantly reduced following
197                                              Osteolytic lesions were successfully quantified using sm
198  metastasis produced detectable, progressive osteolytic lesions within 3 weeks of intracardiac inject
199  those cells with increased IGF-IR form both osteolytic lesions within the tibiae and secondary tumor
200 evented splenomegaly, limited development of osteolytic lesions, and concomitantly reduced tumor grow
201  turn a suppressor of osteoclastic activity, osteolytic lesions, and disease burden in a preclinical
202  correlated with markers of bone resorption, osteolytic lesions, and markers of disease activity.
203 r survival, a smaller tumor burden, and less osteolytic lesions, as compared with mice bearing contro
204 C4-2B's ability to induce mixed osteoblastic/osteolytic lesions, C4-2B cells were stably transfected
205 tumor primarily metastasizes to bone to form osteolytic lesions, causing severe pain and pathological
206                            In cancer-induced osteolytic lesions, cleavage of receptor activator of nu
207 geting osteoclasts, which are upregulated in osteolytic lesions, may facilitate earlier follow-up in
208 acquired immune response could contribute to osteolytic lesions, we injected the periodontal pathogen
209                                          The osteolytic lesions, which develop usually in the long bo
210 frequently metastasize to bone, resulting in osteolytic lesions, yet the underlying mechanisms are po
211  and decrease the progression of established osteolytic lesions.
212 n myeloma cells inhibited the development of osteolytic lesions.
213 mall group of Tax(+) animals presenting with osteolytic lesions.
214 nificantly prevented the formation of severe osteolytic lesions.
215 ant in the resulting suppression of skeletal osteolytic lesions.
216 essential for the formation of premetastatic osteolytic lesions.
217 cell line, C4-2B, induces mixed osteoblastic/osteolytic lesions.
218 te, significantly delayed the progression of osteolytic lesions.
219 alyses to identify molecular determinants of osteolytic lesions.
220 ue associated with progressive periarticular osteolytic lesions.
221  insipidus, bilateral ear discharge, and new osteolytic lesions.
222 with metastatic breast cancer who have known osteolytic lesions.
223 ne among those increased in MM patients with osteolytic lesions.
224 and B-symptoms and was found to have diffuse osteolytic lesions.
225 ssion, radiation or surgery to bone, and new osteolytic lesions.
226 ecrete osteoclastogenic factors that promote osteolytic lesions; however, the identity of these facto
227 MMP-7 and MMP-9 null mice were injected with osteolytic luciferase-tagged mammary tumor cell lines.
228                            Ewing sarcoma, an osteolytic malignancy that mainly affects children and y
229 in level is elevated in multiple myeloma, an osteolytic malignancy, where it might serve as predictiv
230 wed a dramatically impaired capacity to form osteolytic metastases and induce cachexia.
231 n tyrosine phosphorylation induced 74% fewer osteolytic metastases as compared with the control group
232                Breast cancer commonly causes osteolytic metastases in bone, a process that is depende
233 one US and 12 European patients with painful osteolytic metastases involving bone were treated with i
234                       RF ablation of painful osteolytic metastases is safe, and the relief of pain is
235                               RFA of painful osteolytic metastases provides significant pain relief f
236 sms responsible for osteoclast activation in osteolytic metastases should lead to development of nove
237  carcinoma (RCC) patients often present with osteolytic metastases, we aimed to investigate serum scl
238 environment, leading to the establishment of osteolytic metastases.
239 ders such as osteoporosis and contributes to osteolytic metastases.
240 treatment of hypercalcemia of malignancy and osteolytic metastases.
241 ignificantly reduces skeletal morbidity from osteolytic metastases.
242 rapeutic targets to block progression toward osteolytic metastases.
243  studied in detail using an in vivo model of osteolytic metastases.
244 ents with carcinoma of the gall bladder with osteolytic metastasis (stage 4).
245 ths, 12 adult patients with a single painful osteolytic metastasis in whom radiation therapy or chemo
246 mportant regulator of TGF-beta responses and osteolytic metastasis of breast cancer cells.
247  is recommended in women with pain caused by osteolytic metastasis to relieve pain when used concurre
248  their role in tumor-bone interaction during osteolytic metastasis.
249 iation is crucial for improving treatment of osteolytic metastasis.
250  MGUS and suggest that cytokines elevated in osteolytic myeloma also may be associated with bone loss
251 one lesions in cervical cancer seem to be of osteolytic nature.
252 acilitate earlier follow-up in patients with osteolytic or mixed bone metastases.
253                 Biofilm-induced inflammatory osteolytic oral infections, such as periodontitis and pe
254 es is problematic because the lesions can be osteolytic, osteoblastic, or mixed, and imaging modaliti
255 pletely prevented the establishment of mixed osteolytic/osteoblastic tibial tumors, as were observed
256 masked Wnt-mediated osteoblastic activity in osteolytic PC-3 cells, the cells were stably transfected
257 ted tumor formation in the bone, both in the osteolytic PC3 and osteoblastic/osteoclastic mixed C4-2B
258 nol-soluble modulins as aureolysin-degraded, osteolytic peptides that trigger osteoblast cell death a
259  differentiation in an otherwise predominant osteolytic phenomenon.
260 lls for bone and their tendency to induce an osteolytic phenotype are a result of interactions betwee
261 implicated in causing erosive arthritis, the osteolytic phenotypes of multiple myeloma and metastatic
262 ression was higher in cell lines with higher osteolytic potential in vivo.
263       These mutations block the invasive and osteolytic properties of MDA-MB-231 breast cancer cells
264          Overexpression of p45-sErbB3 in the osteolytic prostate cancer cell line PC-3 converted its
265 lization (osteopenia) is coupled to enhanced osteolytic resorption in En1 mutants.
266 bone phenotype, we also observed an enhanced osteolytic response following RANKL injection over the c
267 Fbn2(-/-) mice display a greater than normal osteolytic response to locally implanted lipopolysacchar
268 OC precursors, altering bone homeostasis and osteolytic responses.
269  immune and skeletal systems and suggests an osteolytic role of IL-12 in pathogenesis of periodontal
270 y-one days after intramedullary injection of osteolytic sarcoma cells into the femur, there was exten
271                                              Osteolytic sarcoma cells were implanted into the medulla
272                Higher SUVs were observed for osteolytic than osteoblastic disease (mean, 6.77 and 0.9
273  may provide a new molecular target for anti-osteolytic therapy.
274 genes may be relevant therapeutic targets in osteolytic tumor burden.
275              In vitro analyses revealed that osteolytic tumor cells lack expression of the Hh recepto
276 mor (GCT) of bone is a histologically benign osteolytic tumor featuring prominent osteoclast-like gia
277 ncer pain, the hyperalgesia that occurs with osteolytic tumor growth is associated with the sensitiza
278 ilarly resistant to bone loss resulting from osteolytic tumor growth.
279 ased OC activity on tumor growth in 2 murine osteolytic tumor models.
280 tivity converted the C4-2B cells to a highly osteolytic tumor.
281                                          The osteolytic tumors in the 143B model showed the highest u
282 g Tax (Tax(+)), which spontaneously develops osteolytic tumors throughout the vertebrae and hind limb
283 could effectively target metastasis to bone, osteolytic tumors, and soft tissue tumors.
284  is a very rare, aggressive, and progressive osteolytic tumour for which no standard medicinal treatm
285 hoplasty was efficacious in the treatment of osteolytic vertebral compression fractures resulting fro
286  efficacy of kyphoplasty in the treatment of osteolytic vertebral compression fractures resulting fro
287 rocedures were performed in 18 patients with osteolytic vertebral compression fractures resulting fro
288     PC3 and DU145 bone tumors were primarily osteolytic, whereas LNCaP bone tumors were both osteobla

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