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Cancer metastasis: enactment of the script for human reproductive drama

机译:癌症转移:人类生殖戏剧剧本的制定

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摘要

Based on compelling evidence from many biological disciplines, we put forth a hypothesis for cancer metastasis. In the hypothesis, the metastatic cascade is depicted as human reproduction in miniature. Illustrated in a reproductive light, the staggering resemblance of cancer metastasis to human reproduction becomes evident despite some ostensible dis-similarities. In parallel to the appearance of primordial germ cells during early embryogenesis, the cancer reproductive saga starts with the separation of metastasis initiating cells (MICs) from cancer initiating cells when the primary cancer is still in its infancy. Prime MICs embark on a journey to the host bone marrow where they undergo further development and regulation. Migrating MICs are guided by the same CXCR4/CYCL12 axis as used in the migration of primordial germ cells to the genital ridge. Like the ovary, the host bone marrow features immune privileges, coolness, hypoxia and acidity which are essential for stemness maintenance and regulation. Opportune activation of the MICs via fusion with bone marrow stem cells triggers a frenzy of cellular proliferation and sets them on the move again. This scenario is akin to oocyte fertilization in the Fallopian tube and its subsequent journey towards the decidum. Just as the human reproductive process is plagued with undesirable outcomes so is the cancer metastasis highly inefficient. The climax of the cancer metastatic drama (colonization) is reached when proliferating MIC clusters attempt to settle down on decidum-like premetastatic sites. Successfully colonized clusters blossom into overt macrometastases only after the execution of sophisticated immunomodulation, angiogenesis and vascular remodeling. Similarly, the implanted blastomere needs to orchestrate these feats before flourishing into a new life. What is more, the cancer reproductive drama seems to be directed by a primordial hypothalamus–pituitary–gonad axis. Pursuing this reproductive trail could lead to new frontiers and breakthroughs in cancer research and therapeutics.
机译:基于来自许多生物学学科的令人信服的证据,我们提出了癌症转移的假说。在该假设中,转移级联被描述为人类的缩影。从生殖的角度来看,尽管表面上有些不同,但癌症转移与人类生殖的惊人相似性却变得显而易见。与早期胚胎发生过程中原始生殖细胞的出现平行,癌症生殖传奇始于当原发癌仍处于婴儿期时,将转移起始细胞(MIC)与癌起始细胞分离。初级MIC着手前往宿主骨髓,在此进行进一步的发育和调节。迁移MIC由与原始生殖细胞向生殖the的迁移所使用的CXCR4 / CYCL12轴相同。像卵巢一样,宿主骨髓具有免疫特权,凉爽,缺氧和酸性,这对于保持和调节干度至关重要。通过与骨髓干细胞融合而适度激活MIC会触发疯狂的细胞增殖,并使它们再次移动。这种情况类似于输卵管中的卵母细胞受精及其随后的蜕膜之旅。就像人类生殖过程受到不良后果困扰一样,癌症转移的效率也非常低下。当扩散的MIC簇试图在蜕膜样转移前部位定居时,达到了癌症转移剧情的最高潮(殖民化)。仅在执行复杂的免疫调节,血管生成和血管重塑后,成功定居的簇才会开花成明显的宏观转移。同样,植入的卵裂球需要在繁衍后代才能重新编排这些壮举。更重要的是,癌症生殖戏剧似乎是由下丘脑-垂体-性腺原始轴控制的。追求这种生殖途径可能会导致癌症研究和治疗学的新领域和突破。

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