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F1和F10 B16黑色素瘤变体对热疗的差异敏感性。

Differential sensitivity to hyperthermia of the F1 and F10 B16 melanoma variants.

作者信息

Leibovici J, Klorin G, Huszar M, Hoenig S, Michowitz M

机构信息

Department of Pathology, Sackler Faculty of Medicine, Tel-Aviv University, Israel.

出版信息

Int J Exp Pathol. 1991 Apr;72(2):139-50.

PMID:2015198
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2002304/
Abstract

The currently available antitumoral therapeutic modalities are most often inefficient against metastatic disease. The metastatic phenotype has been shown to be largely determined by cell membrane properties. The cell membrane could therefore be considered as a possible target for antimetastatic drugs. In the present study we examined the effect of hyperthermia (the antitumoral effect of which is based, at least partly, on an action on the cell membrane) on the F1 and F10 variants of B16 melanoma. Cells of the more malignant variant, F10, were found to be markedly more sensitive to hyperthermic treatment than those of the less malignant one, F1. One hour in-vitro treatment by supranormal temperatures (ranging from 40 to 46 degrees C) resulted in a differential effect with regard to both proliferating capacity of the cells in vitro and tumorigenic ability following inoculation to mice. Our present results in the B16 melanoma corroborate data obtained by us in another tumour system, the AKR lymphoma. Study of the effect of membrane-acting agents on tumour variants differing in degree of malignancy might result in the finding of antitumoral agents efficient against advanced cancer.

摘要

目前可用的抗肿瘤治疗方式通常对转移性疾病疗效不佳。已表明转移表型很大程度上由细胞膜特性决定。因此,细胞膜可被视为抗转移药物的一个可能靶点。在本研究中,我们检测了热疗(其抗肿瘤作用至少部分基于对细胞膜的作用)对B16黑色素瘤F1和F10变体的影响。发现恶性程度更高的F10变体细胞比恶性程度较低的F1变体细胞对热疗明显更敏感。超正常温度(40至46摄氏度)体外处理1小时,对体外细胞增殖能力和接种到小鼠后的致瘤能力均产生了差异效应。我们目前在B16黑色素瘤中的研究结果证实了我们在另一个肿瘤系统AKR淋巴瘤中获得的数据。研究作用于细胞膜的药物对恶性程度不同的肿瘤变体的影响,可能会找到对晚期癌症有效的抗肿瘤药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/2002304/0b1c94ccfe31/ijexpath00026-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/2002304/3e398b6fbfaf/ijexpath00026-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/2002304/4b1a5a3d79b2/ijexpath00026-0036-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/2002304/ba740231a6d4/ijexpath00026-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/2002304/0b1c94ccfe31/ijexpath00026-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/2002304/3e398b6fbfaf/ijexpath00026-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/2002304/4b1a5a3d79b2/ijexpath00026-0036-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/2002304/ba740231a6d4/ijexpath00026-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d348/2002304/0b1c94ccfe31/ijexpath00026-0038-a.jpg

相似文献

1
Differential sensitivity to hyperthermia of the F1 and F10 B16 melanoma variants.F1和F10 B16黑色素瘤变体对热疗的差异敏感性。
Int J Exp Pathol. 1991 Apr;72(2):139-50.
2
Effect of hyperthermia and thermochemotherapy on primary and metastatic tumour cells of AKR lymphoma.热疗和热化疗对AKR淋巴瘤原发及转移肿瘤细胞的影响。
Int J Exp Pathol. 1990 Aug;71(4):469-77.
3
Differences in cytotoxic effects of activated murine peritoneal macrophages and J774 monocytic cells on metastatic variants of B16 melanoma.活化的小鼠腹腔巨噬细胞和J774单核细胞对B16黑色素瘤转移变体的细胞毒性作用差异。
J Natl Cancer Inst. 1983 Apr;70(4):717-24.
4
Sensitivity to thermochemotherapy of AKR lymphoma and B16 melanoma variants of malignancy.AKR淋巴瘤和恶性B16黑色素瘤变体对热化疗的敏感性。
Clin Exp Metastasis. 1990 Jan-Feb;8(1):33-46. doi: 10.1007/BF00155591.
5
Extraction of immunogenic and suppressogenic antigens from variants of B16 melanoma exhibiting low or high metastatic potentials.从具有低转移潜能或高转移潜能的B16黑色素瘤变体中提取免疫原性和抑制原性抗原。
Cancer Res. 1983 Nov;43(11):5106-11.
6
Feasibility study of high-temperature thermoseed inductive hyperthermia in melanoma treatment.高温热种子感应热疗治疗黑色素瘤的可行性研究。
Oncol Rep. 2011 Apr;25(4):953-62. doi: 10.3892/or.2011.1143. Epub 2011 Jan 13.
7
Expression of tumor antigen correlated with metastatic potential of Lewis lung carcinoma and B16 melanoma clones in mice.肿瘤抗原的表达与小鼠Lewis肺癌和B16黑色素瘤克隆的转移潜能相关。
Cancer Res. 1986 Nov;46(11):5772-8.
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Sequential chemoimmunotherapy with cisplatin, interferon-beta and interleukin-2 inhibits the growth of B16-F1 melanoma in syngeneic mice.顺铂、β-干扰素和白细胞介素-2序贯化学免疫疗法可抑制同基因小鼠中B16-F1黑色素瘤的生长。
Melanoma Res. 2000 Jun;10(3):223-9.
9
Tumor cell and host properties affecting the implantation and survival of blood-borne metastatic variants of B16 melanoma.影响B16黑色素瘤血行转移变体植入和存活的肿瘤细胞及宿主特性。
Isr J Med Sci. 1978 Jan;14(1):38-50.
10
Suppression of B16 melanoma lung colonization by syngeneic monoclonal antibodies.同基因单克隆抗体对B16黑色素瘤肺转移的抑制作用。
Cancer Res. 1987 May 15;47(10):2696-703.

本文引用的文献

1
Comparison of the malignant potential of 10T 1/2 cells and transformants with their survival responses to hyperthermia and to amphotericin B1.
Cancer Res. 1980 Oct;40(10):3763-7.
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Similarities in cellular inactivation by hyperthermia or by ethanol.热疗或乙醇导致细胞失活的相似性。
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Cholesterol levels inversely reflect the thermal sensitivity of mammalian cells in culture.胆固醇水平与培养的哺乳动物细胞的热敏感性呈负相关。
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Involvement of membranes in cellular responses to hyperthermia.细胞膜在细胞对热疗的反应中的作用。
Radiat Res. 1982 Dec;92(3):433-8.
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Regional emergence of metastatic heterogeneity in a growing tumor.正在生长的肿瘤中转移异质性的区域出现。
Cancer Lett. 1982 Nov-Dec;17(2):153-60. doi: 10.1016/0304-3835(82)90028-3.
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Surface sialic acid reduces attachment of metastatic tumour cells to collagen type IV and fibronectin.表面唾液酸可减少转移性肿瘤细胞与IV型胶原和纤连蛋白的附着。
Nature. 1982 Nov 18;300(5889):274-6. doi: 10.1038/300274a0.
7
Heterogeneity in hyperthermic sensitivities of rat 13762NF mammary adenocarcinoma cell clones of differing metastatic potentials.具有不同转移潜能的大鼠13762NF乳腺腺癌细胞克隆对热疗敏感性的异质性。
Radiat Res. 1982 Sep;91(3):555-63.
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Probing the relationship of membrane "fluidity" to heat killing of cells.
Radiat Res. 1982 Mar;89(3):644-6.
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B16 melanoma cell variants: irreversible inhibition of growth and induction of morphologic differentiation by anthracycline antibiotics.B16黑色素瘤细胞变体:蒽环类抗生素对其生长的不可逆抑制及形态分化诱导
J Natl Cancer Inst. 1982 Apr;68(4):629-38.
10
Direct antitumor effect of high-molecular-weight levan on Lewis lung carcinoma cells in mice.高分子量果聚糖对小鼠Lewis肺癌细胞的直接抗肿瘤作用。
J Natl Cancer Inst. 1980 Aug;65(2):391-6.