Effects of hydroxy safflower Yellow-A on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823 tumors in nude mice
OBJECTIVE：To study the effects of hydroxy safflower yellow A（HSYA） on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823 tumors in nude mice.METHODS：BGC-823 cells were injected subcutaneously into the right anterior armpit of nude mice to establish an animal model of t...
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| Published in | Journal of Traditional Chinese Medicine Vol. 32; no. 2; pp. 243 - 248 |
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| Main Author | |
| Format | Journal Article |
| Language | English |
| Published |
China
01.06.2012
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0255-2922 0254-6272 |
| DOI | 10.1016/S0254-6272(13)60019-9 |
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| Abstract | OBJECTIVE：To study the effects of hydroxy safflower yellow A（HSYA） on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823 tumors in nude mice.METHODS：BGC-823 cells were injected subcutaneously into the right anterior armpit of nude mice to establish an animal model of transplanted tumors.After 24 h,18 nude mice injected with tumor cells were randomized into model,control,and HSYA 0.028 g/L groups,with six mice in each group.Transplanted tumors were excised on day 20.Tumor inhibition ratios were calculated for the transplanted tumors.Pathological changes and capillary angiogenesis in the tumors were observed by light microscopy.RESULTS：Tumors in the model group grew more quickly than those in the control and HSYA groups,with inhibition ratios of 48% and 30%,respectively.The microvessel count in the HSYA group was lower than in the model group（P〈0.01）,and microvessel density was also lower in the HSYA group（P〈0.05）.Pathological changes were more obvious in tumors in the model group compared to the HSYA group.CONCLUSION：HSYA inhibits the growth of transplanted BGC-823 tumors,and its effects on tumor capillary angiogenesis may represent one of the mechanisms responsible for this antineoplastic effect. |
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| AbstractList | To study the effects of hydroxy safflower yellow A (HSYA) on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823 tumors in nude mice.OBJECTIVETo study the effects of hydroxy safflower yellow A (HSYA) on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823 tumors in nude mice.BGC-823 cells were injected subcutaneously into the right anterior armpit of nude mice to establish an animal model of transplanted tumors. After 24 h, 18 nude mice injected with tumor cells were randomized into model, control, and HSYA 0.028 g/L groups, with six mice in each group. Transplanted tumors were excised on day 20. Tumor inhibition ratios were calculated for the transplanted tumors. Pathological changes and capillary angiogenesis in the tumors were observed by light microscopy.METHODSBGC-823 cells were injected subcutaneously into the right anterior armpit of nude mice to establish an animal model of transplanted tumors. After 24 h, 18 nude mice injected with tumor cells were randomized into model, control, and HSYA 0.028 g/L groups, with six mice in each group. Transplanted tumors were excised on day 20. Tumor inhibition ratios were calculated for the transplanted tumors. Pathological changes and capillary angiogenesis in the tumors were observed by light microscopy.Tumors in the model group grew more quickly than those in the control and HSYA groups, with inhibition ratios of 48% and 30%, respectively. The microvessel count in the HSYA group was lower than in the model group (P < 0.01), and microvessel density was also lower in the HSYA group (P < 0.05). Pathological changes were more obvious in tumors in the model group compared to the HSYA group.RESULTSTumors in the model group grew more quickly than those in the control and HSYA groups, with inhibition ratios of 48% and 30%, respectively. The microvessel count in the HSYA group was lower than in the model group (P < 0.01), and microvessel density was also lower in the HSYA group (P < 0.05). Pathological changes were more obvious in tumors in the model group compared to the HSYA group.HSYA inhibits the growth of transplanted BGC-823 tumors, and its effects on tumor capillary angiogenesis may represent one of the mechanisms responsible for this antineoplastic effect.CONCLUSIONHSYA inhibits the growth of transplanted BGC-823 tumors, and its effects on tumor capillary angiogenesis may represent one of the mechanisms responsible for this antineoplastic effect. To study the effects of hydroxy safflower yellow A (HSYA) on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823 tumors in nude mice. BGC-823 cells were injected subcutaneously into the right anterior armpit of nude mice to establish an animal model of transplanted tumors. After 24 h, 18 nude mice injected with tumor cells were randomized into model, control, and HSYA 0.028 g/L groups, with six mice in each group. Transplanted tumors were excised on day 20. Tumor inhibition ratios were calculated for the transplanted tumors. Pathological changes and capillary angiogenesis in the tumors were observed by light microscopy. Tumors in the model group grew more quickly than those in the control and HSYA groups, with inhibition ratios of 48% and 30%, respectively. The microvessel count in the HSYA group was lower than in the model group (P < 0.01), and microvessel density was also lower in the HSYA group (P < 0.05). Pathological changes were more obvious in tumors in the model group compared to the HSYA group. HSYA inhibits the growth of transplanted BGC-823 tumors, and its effects on tumor capillary angiogenesis may represent one of the mechanisms responsible for this antineoplastic effect. OBJECTIVE：To study the effects of hydroxy safflower yellow A（HSYA） on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823 tumors in nude mice.METHODS：BGC-823 cells were injected subcutaneously into the right anterior armpit of nude mice to establish an animal model of transplanted tumors.After 24 h,18 nude mice injected with tumor cells were randomized into model,control,and HSYA 0.028 g/L groups,with six mice in each group.Transplanted tumors were excised on day 20.Tumor inhibition ratios were calculated for the transplanted tumors.Pathological changes and capillary angiogenesis in the tumors were observed by light microscopy.RESULTS：Tumors in the model group grew more quickly than those in the control and HSYA groups,with inhibition ratios of 48% and 30%,respectively.The microvessel count in the HSYA group was lower than in the model group（P〈0.01）,and microvessel density was also lower in the HSYA group（P〈0.05）.Pathological changes were more obvious in tumors in the model group compared to the HSYA group.CONCLUSION：HSYA inhibits the growth of transplanted BGC-823 tumors,and its effects on tumor capillary angiogenesis may represent one of the mechanisms responsible for this antineoplastic effect. |
| Author | 奚胜艳 张前 刘朝阳 解华 岳利峰 高学敏 |
| AuthorAffiliation | Department of Traditional Chinese Medicine of Medical College of Xiamen University;School of Basic Medical Sciences of Beijing University of Chinese Medicine;Tumor research center,Cancer Hospital of Chinese Academy of Medical Sciences |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22876451$$D View this record in MEDLINE/PubMed |
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| Notes | OBJECTIVE：To study the effects of hydroxy safflower yellow A（HSYA） on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823 tumors in nude mice.METHODS：BGC-823 cells were injected subcutaneously into the right anterior armpit of nude mice to establish an animal model of transplanted tumors.After 24 h,18 nude mice injected with tumor cells were randomized into model,control,and HSYA 0.028 g/L groups,with six mice in each group.Transplanted tumors were excised on day 20.Tumor inhibition ratios were calculated for the transplanted tumors.Pathological changes and capillary angiogenesis in the tumors were observed by light microscopy.RESULTS：Tumors in the model group grew more quickly than those in the control and HSYA groups,with inhibition ratios of 48% and 30%,respectively.The microvessel count in the HSYA group was lower than in the model group（P〈0.01）,and microvessel density was also lower in the HSYA group（P〈0.05）.Pathological changes were more obvious in tumors in the model group compared to the HSYA group.CONCLUSION：HSYA inhibits the growth of transplanted BGC-823 tumors,and its effects on tumor capillary angiogenesis may represent one of the mechanisms responsible for this antineoplastic effect. 11-2167/R Hydroxy safflower yellow-A（HSYA） Transplantation tumor BGC-823 CD34 MVD Tumor capillary angiogenesis ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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| Snippet | OBJECTIVE：To study the effects of hydroxy safflower yellow A（HSYA） on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823... To study the effects of hydroxy safflower yellow A (HSYA) on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823 tumors in nude... |
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| SubjectTerms | Adenocarcinoma - blood supply Animals Antineoplastic Agents, Phytogenic - therapeutic use BGC-823 Capillaries - pathology Chalcone - analogs & derivatives Chalcone - therapeutic use Female Humans Male Mice Mice, Inbred BALB C Mice, Nude Neovascularization, Pathologic - drug therapy Quinones - therapeutic use Stomach Neoplasms - blood supply Xenograft Model Antitumor Assays 毛细血管 移植 羟基红花黄色素A 肿瘤血管生成 胃癌 腺癌 裸鼠 |
| Title | Effects of hydroxy safflower Yellow-A on tumor capillary angiogenesis in transplanted human gastric adenocarcinoma BGC-823 tumors in nude mice |
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