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【佳學(xué)基因檢測(cè)】質(zhì)譜成像評(píng)估原發(fā)性口腔癌及其淋巴結(jié)轉(zhuǎn)移的分子瘤內(nèi)異質(zhì)性的預(yù)后價(jià)值

比較做了備注《Molecules》在.?2022 Aug 25;27(17):5458.發(fā)表了一篇題目為《質(zhì)譜成像評(píng)估原發(fā)性口腔癌及其淋巴結(jié)轉(zhuǎn)移的分子瘤內(nèi)異質(zhì)性的預(yù)后價(jià)值》腫瘤靶向藥物治療基因檢測(cè)臨床研究文章。該研究由Agata Kurczyk,?Marta Gawin,?Piotr Paul,?Ewa Chmielik,?Tomasz Rutkowski,?Monika Pietrowska,?Piotr Wid?ak?等完成。促進(jìn)了腫瘤的正確治療與個(gè)性化用藥的發(fā)展,進(jìn)一步強(qiáng)調(diào)了基因信息檢測(cè)與分析的重要性。

佳學(xué)基因檢測(cè)】質(zhì)譜成像評(píng)估原發(fā)性口腔癌及其淋巴結(jié)轉(zhuǎn)移的分子瘤內(nèi)異質(zhì)性的預(yù)后價(jià)值

品牌基因檢測(cè)價(jià)格表還有嗎


比較做了備注《Molecules》在.?2022 Aug 25;27(17):5458.發(fā)表了一篇題目為《質(zhì)譜成像評(píng)估原發(fā)性口腔癌及其淋巴結(jié)轉(zhuǎn)移的分子瘤內(nèi)異質(zhì)性的預(yù)后價(jià)值》腫瘤靶向藥物治療基因檢測(cè)臨床研究文章。該研究由Agata Kurczyk,?Marta Gawin,?Piotr Paul,?Ewa Chmielik,?Tomasz Rutkowski,?Monika Pietrowska,?Piotr Wid?ak?等完成。促進(jìn)了腫瘤的正確治療與個(gè)性化用藥的發(fā)展,進(jìn)一步強(qiáng)調(diào)了基因信息檢測(cè)與分析的重要性。


腫瘤靶向藥物及正確治療臨床研究內(nèi)容關(guān)鍵詞:


癌癥預(yù)后,頭頸部鱗狀細(xì)胞癌,瘤內(nèi)異質(zhì)性,長期結(jié)果,質(zhì)譜成像,腫瘤微環(huán)境


腫瘤靶向治療基因檢測(cè)臨床應(yīng)用結(jié)果


腫瘤內(nèi)異質(zhì)性 (ITH) 的不同方面與癌癥的發(fā)展及其對(duì)治療的反應(yīng)相關(guān),具有推測(cè)的預(yù)后價(jià)值。在這里,我們尋找通過質(zhì)譜成像 (MSI) 分析的表型 ITH 與頭頸癌預(yù)后之間的潛在關(guān)聯(lián)。該研究涉及從 77 名局部晚期口腔鱗狀細(xì)胞癌患者中切除的組織標(biāo)本,其中 37 名患者的原發(fā)腫瘤和同步淋巴結(jié)轉(zhuǎn)移的匹配樣本進(jìn)行了分析。對(duì)所有患者進(jìn)行了 3 年的隨訪,將他們分為兩組:無疾病證據(jù)(NED,n = 41)和疾病進(jìn)展(PD,n = 36)。在組織內(nèi)胰蛋白酶消化后,所有癌癥區(qū)域的肽圖都使用無監(jiān)督的方法進(jìn)行分割,以揭示其內(nèi)在的異質(zhì)性。我們發(fā)現(xiàn) PD 組的腫瘤內(nèi)光譜相似性更高,NED 組在圖像分割過程中識(shí)別的簇的多樣性更高,這表明患者的 ITH 水平更高,結(jié)果更有利。與長期結(jié)果相關(guān)的分子成分的特征可能與參與免疫功能的蛋白質(zhì)有關(guān)。此外,觀察到 ITH 與組織病理學(xué)淋巴細(xì)胞宿主反應(yīng)之間存在正相關(guān)。因此,我們提出在預(yù)后較好的癌癥中,MSI 顯示的 ITH 水平較高可能反映了腫瘤微環(huán)境中異型成分的存在,例如浸潤免疫細(xì)胞增強(qiáng)了對(duì)治療的反應(yīng)。頭頸部鱗狀細(xì)胞癌;瘤內(nèi)異質(zhì)性;長期結(jié)果;質(zhì)譜成像;腫瘤微環(huán)境。


腫瘤發(fā)生與反復(fù)轉(zhuǎn)移國際數(shù)據(jù)庫描述:


Different aspects of intra-tumor heterogeneity (ITH), which are associated with the development of cancer and its response to treatment, have postulated prognostic value. Here we searched for potential association between phenotypic ITH analyzed by mass spectrometry imaging (MSI) and prognosis of head and neck cancer. The study involved tissue specimens resected from 77 patients with locally advanced oral squamous cell carcinoma, including 37 patients where matched samples of primary tumor and synchronous lymph node metastases were analyzed. A 3-year follow-up was available for all patients which enabled their separation into two groups: with no evidence of disease (NED,?n?= 41) and with progressive disease (PD,?n?= 36). After on-tissue trypsin digestion, peptide maps of all cancer regions were segmented using an unsupervised approach to reveal their intrinsic heterogeneity. We found that intra-tumor similarity of spectra was higher in the PD group and diversity of clusters identified during image segmentation was higher in the NED group, which indicated a higher level of ITH in patients with more favorable outcomes. Signature of molecular components that correlated with long-term outcomes could be associated with proteins involved in the immune functions. Furthermore, a positive correlation between ITH and histopathological lymphocytic host response was observed. Hence, we proposed that a higher level of ITH revealed by MSI in cancers with a better prognosis could reflect the presence of heterotypic components of tumor microenvironment such as infiltrating immune cells enhancing the response to the treatment.Keywords:?cancer prognosis; head and neck squamous cell carcinoma; intratumor heterogeneity; long-term outcome; mass spectrometry imaging; tumor microenvironment.



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