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胃饥饿素是乳腺癌的预后标志物和潜在治疗靶点。

Ghrelin is a prognostic marker and a potential therapeutic target in breast cancer.

机构信息

Department of Medical Sciences, Section of Endocrine Oncology, Uppsala University, Uppsala, Sweden.

Department of Oncology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

出版信息

PLoS One. 2017 Apr 18;12(4):e0176059. doi: 10.1371/journal.pone.0176059. eCollection 2017.

Abstract

Ghrelin and obestatin are gastrointestinal peptides, encoded by the same preproghrelin gene. Both are expressed in breast cancer tissue and ghrelin has been implicated in breast cancer tumorigenesis. Despite recent advances in breast cancer management the need for new prognostic markers and potential therapeutic targets in breast cancer remains high. We studied the prognostic impact of ghrelin and obestatin in women with node negative breast cancer. Within a cohort of women with breast cancer with tumor size ≤ 50 mm, no lymph node metastases and no initiation of adjuvant chemotherapy, 190 women were identified who died from breast cancer and randomly selected 190 women alive at the corresponding time as controls. Tumor tissues were immunostained with antibodies versus the peptides. Ghrelin expression was associated with better breast cancer specific survival in univariate analyses (OR 0.55, 95% CI 0.36-0.84) and in multivariate models, adjusted for endocrine treatment and age (OR 0.57, 95% CI 0.36-0.89). Obestatin expression was non-informative (OR 1.2, 95% CI 0.60-2.46). Ghrelin expression is independent prognostic factor for breast cancer death in node negative patients-halving the risk for dying of breast cancer. Our data implies that ghrelin could be a potential therapeutic target in breast cancer treatment.

摘要

胃饥饿素和肥胖抑制素是胃肠道肽,由相同的前胃饥饿素基因编码。两者均在乳腺癌组织中表达,而胃饥饿素被认为与乳腺癌的肿瘤发生有关。尽管乳腺癌的治疗取得了最近的进展,但仍需要新的预后标志物和潜在的治疗靶点。我们研究了胃饥饿素和肥胖抑制素在淋巴结阴性乳腺癌女性中的预后影响。在一组肿瘤大小≤50mm、无淋巴结转移且未开始辅助化疗的乳腺癌女性中,确定了 190 名死于乳腺癌的女性,并随机选择了 190 名同期存活的女性作为对照。使用针对这些肽的抗体对肿瘤组织进行免疫染色。在单因素分析中,胃饥饿素表达与更好的乳腺癌特异性生存相关(OR 0.55,95%CI 0.36-0.84),在调整内分泌治疗和年龄的多因素模型中(OR 0.57,95%CI 0.36-0.89)也是如此。肥胖抑制素表达无信息(OR 1.2,95%CI 0.60-2.46)。胃饥饿素表达是淋巴结阴性患者乳腺癌死亡的独立预后因素-使死于乳腺癌的风险减半。我们的数据表明,胃饥饿素可能是乳腺癌治疗的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c159/5395214/7e979fdcdb14/pone.0176059.g001.jpg

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