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骨橋蛋白(osteopontin,OPN)是驅(qū)動(dòng)乳腺癌復(fù)發(fā)的治療靶點(diǎn)

更新時(shí)間:2025-03-16   點(diǎn)擊次數(shù):119次

中文摘要:

復(fù)發(fā)性乳腺癌通常會(huì)對(duì)標(biāo)準(zhǔn)護(hù)理療法產(chǎn)生耐藥性。確定導(dǎo)致癌癥復(fù)發(fā)的可靶向因素仍然是改善長(zhǎng)期結(jié)果的限速步驟。在這項(xiàng)研究中,我們確定腫瘤細(xì)胞來(lái)源的骨橋蛋白是腫瘤復(fù)發(fā)的自分泌和旁分泌驅(qū)動(dòng)因素。骨橋蛋白促進(jìn)腫瘤細(xì)胞增殖,募集巨噬細(xì)胞,并與 IL-4 協(xié)同作用,使它們進(jìn)一步極化為促腫瘤狀態(tài)。氯膦酸鹽脂質(zhì)體(Liposoma)清除/耗竭巨噬細(xì)胞和抑制骨橋蛋白可減少?gòu)?fù)發(fā)性腫瘤生長(zhǎng)。此外,在原代荷瘤雌性小鼠中靶向骨橋蛋白可防止轉(zhuǎn)移,允許 T 細(xì)胞浸潤(rùn)和激活,并改善抗 PD-1 免疫治療反應(yīng)。臨床上,骨橋蛋白在復(fù)發(fā)性轉(zhuǎn)移性腫瘤中的表達(dá)高于女性患者匹配的原發(fā)性乳腺腫瘤。骨橋蛋白與巨噬細(xì)胞浸潤(rùn)呈正相關(guān),隨著腫瘤分級(jí)的升高而增加,其通路活性升高與預(yù)后不良和長(zhǎng)期復(fù)發(fā)相關(guān)。我們的研究結(jié)果表明了臨床意義和基于骨橋蛋白在乳腺癌進(jìn)展和復(fù)發(fā)中的多軸作用的替代治療策略。

英文摘要:

Recurrent breast cancers often develop resistance to standard-of-care therapies. Identifying targetable factors contributing to cancer recurrence remains the rate-limiting step in improving long-term outcomes. In this study, we identify tumor cell-derived osteopontin as an autocrine and paracrine driver of tumor recurrence. Osteopontin promotes tumor cell proliferation, recruits macrophages, and synergizes with IL-4 to further polarize them into a pro-tumorigenic state. Macrophage depletion and osteopontin inhibition decrease recurrent tumor growth. Furthermore, targeting osteopontin in primary tumor-bearing female mice prevents metastasis, permits T cell infiltration and activation, and improves anti-PD-1 immunotherapy response. Clinically, osteopontin expression is higher in recurrent metastatic tumors versus female patient-matched primary breast tumors. Osteopontin positively correlates with macrophage infiltration, increases with higher tumor grade, and its elevated pathway activity is associated with poor prognosis and long-term recurrence. Our findings suggest clinical implications and an alternative therapeutic strategy based on osteopontin’s multiaxial role in breast cancer progression and recurrence.


論文信息:

論文題目:Osteopontin is a therapeutic target that drives breast cancer recurrence

期刊名稱(chēng):Nature Communications

時(shí)間期卷:15, Article number: 9174 (2024)

在線(xiàn)時(shí)間:2024年10月24日

DOI:doi.org/10.1038/s41467-024-53023-9

產(chǎn)品信息:

貨號(hào):CP-005-005

規(guī)格:5ml+5ml

品牌:Liposoma

產(chǎn)地:荷蘭

名稱(chēng):Clodronate Liposomes and Control Liposomes

辦事處:Target Technology(靶點(diǎn)科技)

Clodronate Liposomes氯膦酸鹽脂質(zhì)體助力乳腺癌模型研究,荷蘭Liposoma巨噬細(xì)胞清除劑Clodronate Liposomes見(jiàn)刊于Nature Communications:骨橋蛋白(osteopontin,OPN)是驅(qū)動(dòng)乳腺癌復(fù)發(fā)的治療靶點(diǎn)


氯膦酸二鈉脂質(zhì)體清除巨噬細(xì)胞助力乳腺癌瘤模型腫瘤免疫研究

骨橋蛋白(osteopontin,OPN)是驅(qū)動(dòng)乳腺癌復(fù)發(fā)的治療靶點(diǎn)


Liposoma巨噬細(xì)胞清除劑Clodronate Liposomes氯膦酸二鈉脂質(zhì)體的材料和方法:

骨橋蛋白(osteopontin,OPN)是驅(qū)動(dòng)乳腺癌復(fù)發(fā)的治療靶點(diǎn)


Macrophage depletion by clodronate liposomes

MIC β1KO mice were induced until palpable “recurrent" tumors reached 50?mm3 after their primary dormancy from weekly palpations. Tumor-bearing mice were given 10?μL per gram of either PBS- or clodronate-liposomes (LIPOSOMA, Batch P03M0124 and C6M0224, respectively) three times per week through intraperitoneal injections. All mice were given 10 doses.


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