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The spreading progression was not much affected by the presence of concrete and sparging gases.
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In contrast, when NHDF were magnetically labeled and patterned together with MCF10A/myr-Akt1 (direct-interaction array), spreading and progression were observed along with NHDF.
FAK regulates major cellular functions including migration, spreading, cell cycle progression and survival in numerous cell types [ 21].
The underlying thesis in solid tumor biology is that metastasis generally begins with an orderly progression, spreading through the lymphatic channels to the SLN that should be reflected in the pathological status of the subsequent lymph nodes.
Metabolic alterations constitute a hallmark in cancer cells: They are required for driving transformation, progression and spreading cancer in tissues [16].
IL-12 treatment of NBEC reduced significantly their ability to release some cytokines/chemokines that have been shown to be involved in NSCLC angiogenesis, progression and spreading [31] [36] such as, for example, MCP-1/CCL2 and IL-6 [37].
However, the increase of proteolytic activity in cancer lesions is universally recognized as a hallmark of cancer progression and spreading.
Epitope spreading correlated with disease progression from an acute onset at day 10 to 14 to a chronic phase at day 28 and 67.
The interaction between cytokines, chemokines, growth factors and their receptors forms a comprehensive network at the tumor site, which is primary responsible for overall tumor progression and spreading or induction of antitumor immune responses and tumor rejection [ 5].
Other mechanisms responsible for stimulation of tumour progression and spreading by tumour-derived NO are stimulation of tumour cell invasiveness Orucevic et al, 1999; Jadeski et al, 2000) as well as increased expression of angiogenic factors (Morbidelli et al, 2001; Feng et al, 2002).
In conclusion, this is the first report on the concomitant involvement of CXCR4 and CXCR7 receptors both transducing on the mTOR pathway, affecting progression and spreading of human renal cancer cells suggesting that targeting CXCR4, CXCR7 and mTOR may improve therapeutic efficacy and prevent mTOR-targeting agents' resistance.
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