Melanoma Controls the Metastatic Process only in Terms of Metastatic Cell Dissemination - What Is Responsible for Metastatic Cell Proliferation?

IF 0.6 4区 医学 Q4 DERMATOLOGY
Acta Dermatovenerologica Croatica Pub Date : 2021-04-01
Leo Čabrijan, Jasna Lipozenčić
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引用次数: 0

Abstract

The process of melanoma metastasis can be divided into two stages of metastatic cell dissemination and proliferation. The whole process should be observed and distinguished through the variable or prism of time. The fact that melanoma metastases are detected in visceral organs at the stage when they are macroscopically visible does not imply that their onset has occurred much earlier. Additionally, it is quite obvious that the entire process is not driven by melanoma but rather only the initial stage of metastatic cell dissemination, whereas the later stage of metastatic cell proliferation is driven by other factors, firstly by mutated genes in the presence of melanoma or without it. Dissemination of metastatic cells occurs at approximately the same time in all melanomas, at MIS transition to MM, but is not immediately followed by metastatic cell proliferation; instead, some time has to elapse for a particular gene mutation to occur, and this timing varies among melanomas. Following dissemination of metastatic cells to visceral organs, they remain inactive, and in this period the presence of melanoma is not necessary anymore for metastatic cell proliferation, as they are waiting for a signal to start multiplying. This is clearly discernible from the fact that melanoma is today detected and removed frequently and early, but visible metastases then develop in the absence of melanoma, which may also regress spontaneously. Accordingly, MM is no longer necessary for metastasis later on. Finally, let me rephrase the title: melanoma is only responsible for initial dissemination of metastatic cells, whereas subsequent proliferation of metastatic cells is driven by other factors, most probably mutated genes.

黑色素瘤仅在转移细胞扩散方面控制转移过程-什么是转移细胞增殖的原因?
黑色素瘤的转移过程可分为转移细胞播散和增殖两个阶段。整个过程应该通过变量或时间棱镜来观察和区分。黑色素瘤转移在肉眼可见的内脏器官中被发现,这一事实并不意味着它的发病时间要早得多。此外,很明显,整个过程不是由黑色素瘤驱动的,而只是转移细胞传播的初始阶段,而转移细胞增殖的后期是由其他因素驱动的,首先是存在黑色素瘤或不存在黑色素瘤时基因突变。在所有黑色素瘤中,转移细胞的播散几乎发生在同一时间,即从MIS向MM过渡,但不会立即发生转移细胞增殖;相反,一个特定的基因突变必须经过一段时间才能发生,而这个时间在黑色素瘤中是不同的。在转移细胞扩散到内脏器官后,它们保持不活跃状态,在此期间,黑色素瘤的存在不再是转移细胞增殖的必要条件,因为它们正在等待开始繁殖的信号。这一点可以从以下事实中清楚地看出:如今黑色素瘤经常被及早发现并切除,但在没有黑色素瘤的情况下,会出现可见的转移,这种转移也可能自发消退。因此,MM不再是以后转移所必需的。最后,让我重新表述一下标题:黑色素瘤只负责转移细胞的初始传播,而随后转移细胞的增殖是由其他因素驱动的,最有可能是突变的基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Dermatovenerologica Croatica
Acta Dermatovenerologica Croatica 医学-皮肤病学
CiteScore
0.60
自引率
0.00%
发文量
23
审稿时长
>12 weeks
期刊介绍: Acta Dermatovenerologica Croatica (ADC) aims to provide dermatovenerologists with up-to-date information on all aspects of the diagnosis and management of skin and venereal diseases. Accepted articles regularly include original scientific articles, short scientific communications, clinical articles, case reports, reviews, reports, news and correspondence. ADC is guided by a distinguished, international editorial board and encourages approach to continuing medical education for dermatovenerologists.
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